The present disclosure generally relates to ultrasonic surgical systems, electrosurgical systems, and combination electrosurgical/ultrasonic systems for performing surgical procedures such as coagulating, sealing, and/or cutting tissue. In particular, the present disclosure relates to customized algorithms for performing such procedures based on the type of tissue being treated. More particularly, the present disclosure relates to a generator which digitally generates electrical signal waveforms for surgical instruments used to perform such procedures. The digital electrical signal waveforms are stored in a lookup table. The generator digitally generates multiple electrical signal waveforms to drive multiple ultrasonic transducers.
Ultrasonic surgical instruments are finding increasingly widespread applications in surgical procedures by virtue of the unique performance characteristics of such instruments. Depending upon specific instrument configurations and operational parameters, ultrasonic surgical instruments can provide substantially simultaneous cutting of tissue and hemostasis by coagulation, desirably minimizing patient trauma. The cutting action is typically realized by an-end effector, or blade tip, at the distal end of the instrument, which transmits ultrasonic energy to tissue brought into contact with the end effector. Ultrasonic instruments of this nature can be configured for open surgical use, laparoscopic, or endoscopic surgical procedures including robotic-assisted procedures.
Some surgical instruments utilize ultrasonic energy for both precise cutting and controlled coagulation. Ultrasonic energy cuts and coagulates by vibrating a blade in contact with tissue. Vibrating at high frequencies (e.g., 55,500 times per second), the ultrasonic blade denatures protein in the tissue to form a sticky coagulum. Pressure exerted on tissue with the blade surface collapses blood vessels and allows the coagulum to form a hemostatic seal. The precision of cutting and coagulation is controlled by the surgeon's technique and adjusting the power level, blade edge, tissue traction, and blade pressure.
Electrosurgical devices for applying electrical energy to tissue in order to treat and/or destroy the tissue are also finding increasingly widespread applications in surgical procedures. An electrosurgical device typically includes a handpiece, an instrument having a distally-mounted end effector (e.g., one or more electrodes). The end effector can be positioned against the tissue such that electrical current is introduced into the tissue. Electrosurgical devices can be configured for bipolar or monopolar operation. During bipolar operation, current is introduced into and returned from the tissue by active and return electrodes, respectively, of the end effector. During monopolar operation, current is introduced into the tissue by an active electrode of the end effector and returned through a return electrode (e.g., a grounding pad) separately located on a patient's body. Heat generated by the current flowing through the tissue may form hemostatic seals within the tissue and/or between tissues and thus may be particularly useful for sealing blood vessels, for example. The end effector of an electrosurgical device also may include a cutting member that is movable relative to the tissue and the electrodes to transect the tissue.
Electrical energy applied by an electrosurgical device can be transmitted to the instrument by a generator in communication with the handpiece. The electrical energy may be in the form of radio frequency (RF) energy that may be in a frequency range described in EN 60601-2-2:2009+A11:2011, Definition 201.3.218—HIGH FREQUENCY. For example, the frequencies in monopolar RF applications are typically restricted to less than 5 MHz. However, in bipolar RF applications, the frequency can be almost anything. Frequencies above 200 kHz can be typically used for MONOPOLAR applications in order to avoid the unwanted stimulation of nerves and muscles which would result from the use of low frequency current. Lower frequencies may be used for BIPOLAR techniques if the RISK ANALYSIS shows the possibility of neuromuscular stimulation has been mitigated to an acceptable level. Normally, frequencies above 5 MHz are not used in order to minimize the problems associated with HIGH FREQUENCY LEAKAGE CURRENTS. However, higher frequencies may be used in the case of BIPOLAR techniques. It is generally recognized that 10 mA is the lower threshold of thermal effects on tissue.
In application, an electrosurgical device can transmit low frequency RF energy through tissue, which causes ionic agitation, or friction, in effect resistive heating, thereby increasing the temperature of the tissue. Because a sharp boundary is created between the affected tissue and the surrounding tissue, surgeons can operate with a high level of precision and control, without sacrificing un-targeted adjacent tissue. The low operating temperatures of RF energy is useful for removing, shrinking, or sculpting soft tissue while simultaneously sealing blood vessels. RF energy works particularly well on connective tissue, which is primarily comprised of collagen and shrinks when contacted by heat.
Other electrical surgical instruments include, without limitation, irreversible and/or reversible electroporation, and/or microwave technologies, among others. Accordingly, the techniques disclosed herein are applicable to ultrasonic, bipolar or monopolar RF (electrosurgical), irreversible and/or reversible electroporation, and/or microwave based surgical instruments, among others.
A challenge of using these medical devices is the inability to control and customize the power output depending on the type of tissue being treated by the devices. It would be desirable to provide a surgical instrument that overcomes some of the deficiencies of current instruments. The surgical system described herein overcomes those deficiencies.
As disclosed herein, a generator may be configured to generate an output waveform digitally and provide it to a surgical instrument such that the surgical instrument may utilize the waveform for various tissue effects. The present disclosure provides for generator capabilities that promote tissue effects via wave-shaping and that drive RF and Ultrasonic energy simultaneously to a single surgical instrument or multiple surgical instruments.
Conventional generators for ultrasonic surgical instruments are configured to drive a single ultrasonic transducer. Shortcomings of such conventional ultrasonic generators is the inability to drive multiple ultrasonic transducers in one or more instruments simultaneously. Other shortcomings include the inability of ultrasonic generators to drive multiple vibration modes in one instrument to achieve longer active length at the tip of an ultrasonic blade to provide various tissue effects.
As disclosed herein, a generator may be configured to generate an output waveform digitally and provide it to a surgical instrument such that the surgical instrument may utilize the waveform for various tissue effects. The present disclosure provides for generator capabilities that promote tissue effects via wave-shaping and that drive RF and Ultrasonic energy simultaneously to a single surgical instrument or multiple surgical instruments. The present disclosure also provides a generator configured to generate wave-shaping to protect electrical output components of the generator when driving simultaneous RF and Ultrasonic waveforms.
In one aspect, a method of generating electrical signal waveforms by a generator is provided. The generator comprises a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit. The memory circuit defines a lookup table. The method comprises storing, by the digital processing circuit, phase points of a digital electrical signal waveform in the lookup table defined by the memory circuit, wherein the digital electrical signal waveform is represented by a predetermined number of phase points, wherein the predetermined number phase points define a predetermined wave shape; receiving a clock signal by the digital synthesis circuit, and at each clock cycle: retrieving, by the digital processing circuit, a phase point from the lookup table; and converting, by the DAC circuit, the retrieved phase point to an analog signal.
In another aspect, a method of generating electrical signal waveforms by a generator is provided. The generator comprises a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, where the memory circuit defines first and second lookup tables. The method comprises storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; receiving, by the digital synthesis circuit, a clock signal, and at each clock cycle: retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; and determining, by the digital processing circuit, whether to switch between the phase points of the first and second electrical signal waveforms or to synchronize the phase points of the first and second electrical signal waveforms.
In yet another a generator for generating electrical signal waveforms is provided. The generator comprises a digital processing circuit; a memory circuit in communication with the digital processing circuit, the memory circuit defining a lookup table; a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, the digital synthesis circuit receiving a clock signal; and a digital-to-analog converter (DAC) circuit. The digital processing circuit configured to store phase points of a digital electrical signal waveform in the lookup table defined by the memory circuit, wherein the digital electrical signal waveform is represented by a predetermined number of phase points, wherein the predetermined number phase points define a predetermined wave shape; and retrieve a phase point from the lookup table at each clock cycle; and the DAC circuit configured to convert the retrieved phase point to an analog signal.
In one aspect, a method of generating electrical signal waveforms by a generator is provided. The generator comprises a digital processing circuit, a memory circuit in communication with the digital processing circuit, the memory circuit defining first and second lookup tables, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC). The method comprises storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; and receiving a clock signal by the digital synthesis circuit, and at each clock cycle retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; combining, by the digital processing circuit, the phase point from the first lookup table with the phase point from the second lookup table to generate a combined phase point; and converting, by the DAC circuit, the combined phase point into an analog signal; wherein the analog signal is configured to drive a first and second ultrasonic transducer.
In another aspect, a method of generating electrical signal waveforms by a generator is provided. The generator comprises a digital processing circuit, a memory circuit in communication with the digital processing circuit, the memory circuit defining first and second lookup tables, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit. The method comprises storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; and receiving a clock signal by the digital synthesis circuit, and at each clock cycle retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; combining, by the digital processing circuit, the phase point from the first lookup table with the phase point from the second lookup table to generate a combined phase point; and converting, by the DAC circuit, the combined phase point into an analog signal; wherein the analog signal is configured to drive a plurality of ultrasonic operational modes of an ultrasonic device.
In yet another a generator for generating electrical signal waveforms is provided. The generator comprises a digital processing circuit; a memory circuit in communication with the digital processing circuit, the memory circuit defining a lookup table; a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, the digital synthesis circuit receiving a clock signal; and a digital-to-analog converter (DAC) circuit; the digital processing circuit configured to: store phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; and store phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; at each clock cycle the digital synthesis circuit is configured to: retrieve a phase point from the first lookup table; retrieve a phase point from the second lookup table; the digital processing circuit configured to: combine the phase point from the first lookup table with the phase point from the second lookup table to generate a combined phase point; and the DAC circuit is configured to convert the combined phase point into an analog signal; wherein the analog signal is configured to drive a first and second ultrasonic transducer.
In one aspect, a method of generating electrical signal waveforms by a generator is provided. The generator comprises a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the memory circuit defining first and second lookup tables, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; receiving, by the digital synthesis circuit, a clock signal, and at each clock cycle; retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; combining, by the digital processing circuit, the first and second digital electrical signal waveforms to form a combined digital electrical signal waveform; and modifying, by the digital processing circuit, the combined digital electrical signal waveform to form a modified digital electrical signal waveform, wherein a peak amplitude of the modified digital electrical signal waveform does not exceed a predetermined amplitude value.
In another aspect, a method of generating electrical signal waveforms by a generator is provided. The generator comprises a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the memory circuit defining first and second lookup tables, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape, wherein the second digital electrical signal waveform is a function of the first digital electrical signal waveform; receiving, by the digital synthesis circuit, a clock signal, and at each clock cycle; retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; combining, by the digital processing circuit, the first and second digital electrical signal waveforms to form a combined digital electrical signal waveform; and modifying, by the digital processing circuit, the combined digital electrical signal waveform to form a modified digital electrical signal waveform, wherein a peak amplitude of the modified digital electrical signal waveform does not exceed a predetermined amplitude value.
In yet another a generator for generating electrical signal waveforms is provided. The generator comprises a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the memory circuit defining first and second lookup tables, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape, wherein the second digital electrical signal waveform is a function of the first digital electrical signal waveform; receiving, by the digital synthesis circuit, a clock signal, and at each clock cycle; retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; modifying, by the digital processing circuit, a frequency of the first digital electrical signal waveform to form a frequency modified first digital electrical signal waveform; and combining, by the digital processing circuit, the frequency modified first digital electrical signal waveform and the second digital electrical signal waveform to form a combined digital electrical signal waveform.
The novel features of the described forms are set forth with particularity in the appended claims. The described forms, however, both as to organization and methods of operation, may be best understood by reference to the following description, taken in conjunction with the accompanying drawings in which:
Before explaining various forms of surgical instruments in detail, it should be noted that the illustrative forms are not limited in application or use to the details of construction and arrangement of parts illustrated in the accompanying drawings and description. The illustrative forms may be implemented or incorporated in other forms, variations and modifications, and may be practiced or carried out in various ways. Further, unless otherwise indicated, the terms and expressions employed herein have been chosen for the purpose of describing the illustrative forms for the convenience of the reader and are not for the purpose of limitation thereof.
Further, it is understood that any one or more of the following-described forms, expressions of forms, examples, can be combined with any one or more of the other following-described forms, expressions of forms, and examples.
Various forms are directed to improved ultrasonic and/or RF electrosurgical instruments configured for effecting tissue dissecting, cutting, and/or coagulation during surgical procedures. In one form, an ultrasonic and/or RF electrosurgical instruments may be configured for use in open surgical procedures, but has applications in other types of surgery, such as laparoscopic, endoscopic, and robotic-assisted procedures. Versatile use is facilitated by selective use of ultrasonic energy.
This application is related to the following commonly owned patent application filed Sep. 14, 2016:
This application also is related to the following commonly owned patent applications filed on Sep. 7, 2016:
This application also is related to the following commonly owned patent applications filed on Jun. 9, 2016:
The various forms will be described in combination with an ultrasonic instrument as described herein. Such description is provided by way of example, and not limitation, and is not intended to limit the scope and applications thereof. For example, any one of the described forms is useful in combination with a multitude of ultrasonic instruments including those described in, for example, U.S. Pat. Nos. 5,938,633; 5,935,144; 5,944,737; 5,322,055; 5,630,420; and 5,449,370, which are each incorporated by reference herein in their entirety.
As will become apparent from the following description, it is contemplated that forms of the surgical instruments described herein may be used in association with an oscillator unit of a surgical system, whereby ultrasonic energy from the oscillator unit provides the desired ultrasonic actuation for the present surgical instrument. It is also contemplated that forms of the surgical instrument described herein may be used in association with a signal generator unit of a surgical system, whereby RF electrical energy, for example, is used to provide feedback to the user regarding the surgical instrument. The ultrasonic oscillator and/or the signal generator unit may be non-detachably integrated with the surgical instrument or may be provided as separate components, which can be electrically attachable to the surgical instrument.
One form of the present surgical apparatus is particularly configured for disposable use by virtue of its straightforward construction. However, it is also contemplated that other forms of the present surgical instrument can be configured for non-disposable or multiple uses. Detachable connection of the present surgical instrument with an associated oscillator and signal generator unit is presently disclosed for single-patient use for illustrative purposes only. However, non-detachable integrated connection of the present surgical instrument with an associated oscillator and/or signal generator unit is also contemplated. Accordingly, various forms of the presently described surgical instruments may be configured for single use and/or multiple use with either detachable and/or non-detachable integral oscillator and/or signal generator unit, without limitation, and all combinations of such configurations are contemplated to be within the scope of the present disclosure.
In one aspect, the desired wave shape may be digitized by 1024 phase points, which are stored in a table, such as, for example, a direct digital synthesis table with a field programmable gate array (FPGA) of the generator. The generator software and digital controls command the FPGA to scan the addresses in this table at the frequency of interest which in turn provides varying digital input values to a DAC circuit that feeds to power amplifier. This method enables generating practically any (or many) types of wave shapes fed into tissue. Furthermore, multiple wave shape tables can be created, stored and applied to tissue.
According to various aspects, a method comprises creating various types of lookup tables in memory such as lookup tables generated by direct digital synthesis (DDS) circuit and stored within FPGAs, for example. Waveforms may be stored in the DDS table or tables as particular wave shapes. Examples of wave shapes in the RF/Electrosurgery tissue treatment field include high crest factor RF signals, which may be used for surface coagulation in an RF mode, for example, low crest factor RF signals, which may be used for deeper penetration into tissue in an RF mode, for example, and waveforms that promote efficient touch-up coagulation, for example. In one aspect, the crest factor (CF) may be defined as the ratio of the peak signal to the root-mean-square (RMS) signal.
The present disclosure provides for the creation of multiple wave shape tables that allow for switching on the fly, either manually or automatically, between the wave shapes based on tissue effect desired. Switching could be based on tissue parameters, such as, for example, tissue impedance and/or other factors. In addition to a traditional sine wave shape, in one aspect a generator may be configured to provide a wave shape that maximizes the power into tissue per cycle. According to one aspect, the wave shape may be a trapezoid wave, a sine or cosine wave, a square wave, a triangle wave, or any combination thereof. In one aspect, a generator may be configured to provide a wave shape or shapes that are synchronized in such way that they make maximizing power delivery in the case that both RF and ultrasonic energy modalities are driven, either simultaneously or sequentially. In one aspect, a generator may be configured to provide a waveform that drives both ultrasonic and RF therapeutic energy simultaneously while maintaining ultrasonic frequency lock. In one aspect, the generator may contain or be associated with a device that provides a circuit topology that enables simultaneously driving RF and ultrasonic energy. In one aspect, a generator may be configured to provide custom wave shapes that are specific to a surgical instrument and the tissue effects provided by such a surgical instrument. Furthermore, the waveforms may be stored in a generator non-volatile memory or in an instrument memory, such as, for example, an electrically erasable programmable read-only memory (EEPROM). The waveform or waveforms may be fetched upon instrument connection to a generator.
With reference to
According to various forms, the generator 100 may be configurable for use with different surgical instruments of different types including, for example, ultrasonic surgical instruments 104, RF electrosurgical instruments 106, and multifunction surgical instruments 108 that integrate RF and ultrasonic energies delivered simultaneously from the generator 100. Although in the form of
Still with reference to
Still with reference to
With reference to both
With reference now to
Still with reference to
In certain forms, a two-position switch may be provided as an alternative to a toggle button 137c. For example, the multifunction surgical instrument 108 may include a toggle button 137a for producing a continuous output at a maximum power level and a two-position toggle button 137b. In a first detented position, toggle button 137b may produce a continuous output at a less than maximum power level, and in a second detented position the toggle button 137b may produce a pulsed output (e.g., at either a maximum or less than maximum power level, depending upon the EEPROM settings). Any one of the buttons 137a, 137b, 137c may be configured to activate RF energy and apply the RF energy to the end effector 125.
Still with reference to
In other forms, the electrical outputs of the ultrasonic drive circuit 114 and the electrosurgery/RF drive circuit 116 may be combined into a single electrical signal capable of driving the multifunction surgical instrument 108 simultaneously with electrosurgical RF and ultrasonic energies. This single electrical drive signal may be produced by the combination drive circuit 118. The multifunction surgical instrument 108 comprises an ultrasonic transducer 120 coupled to an ultrasonic blade and one or more electrodes in the end effector 125 to receive ultrasonic and electrosurgical RF energy. The multifunction surgical instrument 108 comprises signal processing components to split the combined RF/ultrasonic energy signal such that the RF signal can be delivered to the electrodes in the end effector 125 and the ultrasonic signal can be delivered to the ultrasonic transducer 120.
In accordance with the described forms, the ultrasonic drive circuit 114 may produce a drive signal or signals of particular voltages, currents, and frequencies, e.g., 55,500 cycles per second (Hz). The drive signal or signals may be provided to the ultrasonic surgical instrument 104, and specifically to the ultrasonic transducer 120, which may operate, for example, as described above. The ultrasonic transducer 120 and a waveguide extending through the shaft 126 (waveguide not shown) may collectively form an ultrasonic drive system driving an ultrasonic blade 128 of an end effector 122. In one form, the generator 100 may be configured to produce a drive signal of a particular voltage, current, and/or frequency output signal that can be stepped or otherwise modified with high resolution, accuracy, and repeatability.
The generator 100 may be activated to provide the drive signal to the ultrasonic transducer 120 in any suitable manner. For example, the generator 100 may comprise a foot switch 130 coupled to the generator 100 via a foot switch cable 132. A clinician may activate the ultrasonic transducer 120 by depressing the foot switch 130. In addition, or instead of the foot switch 130 some forms of the ultrasonic surgical instrument 104 may utilize one or more switches positioned on the handpiece that, when activated, may cause the generator 100 to activate the ultrasonic transducer 120. In one form, for example, the one or more switches may comprise a pair of toggle buttons 137a, 137b (
Additionally or alternatively, the one or more switches may comprise a toggle button 137c that, when depressed, causes the generator 100 to provide a pulsed output. The pulses may be provided at any suitable frequency and grouping, for example. In certain forms, the power level of the pulses may be the power levels associated with toggle buttons 137a, 137b (maximum, less than maximum), for example.
It will be appreciated that the ultrasonic surgical instrument 104 and/or the multifunction surgical instrument 108 may comprise any combination of the toggle buttons 137a, 137b, 137c. For example, the multifunction surgical instrument 108 could be configured to have only two toggle buttons: a toggle button 137a for producing maximum ultrasonic energy output and a toggle button 137c for producing a pulsed output at either the maximum or less than maximum power level. In this way, the drive signal output configuration of the generator 100 could be 5 continuous signals and 5 or 4 or 3 or 2 or 1 pulsed signals. In certain forms, the specific drive signal configuration may be controlled based upon, for example, EEPROM settings in the generator 100 and/or user power level selection(s).
In certain forms, a two-position switch may be provided as an alternative to a toggle button 137c. For example, the ultrasonic surgical instrument 104 may include a toggle button 137a for producing a continuous output at a maximum power level and a two-position toggle button 137b. In a first detented position, toggle button 137b may produce a continuous output at a less than maximum power level, and in a second detented position the toggle button 137b may produce a pulsed output (e.g., at either a maximum or less than maximum power level, depending upon the EEPROM settings).
In accordance with the described forms, the electrosurgery/RF drive circuit 116 may generate a drive signal or signals with output power sufficient to perform bipolar electrosurgery using RF energy. In bipolar electrosurgery applications, the drive signal may be provided, for example, to electrodes located in the end effector 124 of the RF electrosurgical instrument 106, for example. Accordingly, the generator 100 may be configured for therapeutic purposes by applying electrical energy to the tissue sufficient for treating the tissue (e.g., coagulation, cauterization, tissue welding). The generator 100 may be configured for sub-therapeutic purposes by applying electrical energy to the tissue for monitoring parameters of the tissue during a procedure.
As previously discussed, the combination drive circuit 118 may be configured to drive both ultrasonic and RF electrosurgical energies. The ultrasonic and RF electrosurgical energies may be delivered though separate output ports of the generator 100 as separate signals or though a single port of the generator 100 as a single signal that is a combination of the ultrasonic and RF electrosurgical energies. In the latter case, the single signal can be separated by circuits located in the surgical instruments 104, 106, 108.
The surgical instruments 104, 106, 108 additionally or alternatively may comprise a switch to indicate a position of a jaw closure trigger for operating jaws of the end effector 122, 124, 125. Also, in some forms, the generator 100 may be activated based on the position of the jaw closure trigger, (e.g., as the clinician depresses the jaw closure trigger to close the jaws, ultrasonic energy may be applied).
The generator 100 may comprise an input device 110 (
The generator 100 also may comprise an output device 112 (
Although certain modules and/or blocks of the generator 100 may be described by way of example, it can be appreciated that a greater or lesser number of modules and/or blocks may be used and still fall within the scope of the forms. Further, although various forms may be described in terms of modules and/or blocks to facilitate description, such modules and/or blocks may be implemented by one or more hardware components, e.g., processors, Digital Signal Processors (DSPs), Programmable Logic Devices (PLDs), Application Specific Integrated Circuits (ASICs), circuits, registers and/or software components, e.g., programs, subroutines, logic and/or combinations of hardware and software components. Also, in some forms, the various modules described herein may be implemented utilizing similar hardware positioned within the surgical instruments 104, 106, 108 (i.e., the external generator 100 may be omitted).
In one form, the ultrasonic drive circuit 114, electrosurgery/RF drive circuit 116, and/or the combination drive circuit 118 may comprise one or more embedded applications implemented as firmware, software, hardware, or any combination thereof. The drive circuits 114, 116, 118 may comprise various executable modules such as software, programs, data, drivers, application program interfaces (APIs), and so forth. The firmware may be stored in nonvolatile memory (NVM), such as in bit masked read-only memory (ROM) or flash memory. In various implementations, storing the firmware in ROM may preserve flash memory. The NVM may comprise other types of memory including, for example, programmable ROM (PROM), erasable programmable ROM (EPROM), EEPROM, or battery backed random-access memory (RAM) such as dynamic RAM (DRAM), Double-Data-Rate DRAM (DDRAM), and/or synchronous DRAM (SDRAM).
In one form, the drive circuits 114, 116, 118 comprise a hardware component implemented as a processor for executing program instructions for monitoring various measurable characteristics of the surgical instruments 104, 106, 108 and generating a corresponding output control signals for operating the surgical instruments 104, 106, 108. In forms in which the generator 100 is used in conjunction with the multifunction surgical instrument 108, the output control signal may drive the ultrasonic transducer 120 in cutting and/or coagulation operating modes. Electrical characteristics of the multifunction surgical instrument 108 and/or tissue may be measured and used to control operational aspects of the generator 100 and/or provided as feedback to the user. In forms in which the generator 100 is used in conjunction with the multifunction surgical instrument 108, the output control signal may supply electrical energy (e.g., RF energy) to the end effector 125 in cutting, coagulation and/or desiccation modes. Electrical characteristics of the multifunction surgical instrument 108 and/or tissue may be measured and used to control operational aspects of the generator 100 and/or provide feedback to the user. In various forms, as previously discussed, the hardware component may be implemented as a DSP, PLD, ASIC, circuits, and/or registers. In one form, the processor may be configured to store and execute computer software program instructions to generate the output signals for driving various components of the surgical instruments 104, 106, 108, such as the ultrasonic transducer 120 and the end effectors 122, 124, 125.
Forms of the generator 100 do not rely on a tuning inductor Lt to monitor the motional branch current Im. Instead, the generator 100 may use the measured value of the static capacitance Co in between applications of power for a specific ultrasonic surgical instrument 104 (along with drive signal voltage and current feedback data) to determine values of the motional branch current Im on a dynamic and ongoing basis (e.g., in real-time). Such forms of the generator 100 are therefore able to provide virtual tuning to simulate a system that is tuned or resonant with any value of static capacitance Co at any frequency, and not just at single resonant frequency dictated by a nominal value of the static capacitance Co.
In certain forms, the ultrasonic and electrosurgical drive signals may be provided simultaneously to distinct surgical instruments and/or to a single surgical instrument having the capability to deliver both ultrasonic and electrosurgical energy to tissue, such as the multifunction surgical instrument 108 (
The non-isolated stage 204 may comprise a power amplifier 212 having an output connected to a primary winding 214 of the power transformer 206. In certain forms the power amplifier 212 may be comprise a push-pull amplifier. For example, the non-isolated stage 204 may further comprise a logic device 216 for supplying a digital output to a DAC circuit 218, which in turn supplies a corresponding analog signal to an input of the power amplifier 212. In certain forms the logic device 216 may comprise a programmable gate array (PGA), a FPGA, programmable logic device (PLD), among other logic circuits, for example. The logic device 216, by virtue of controlling the input of the power amplifier 212 via the DAC circuit 218, may therefore control any of a number of parameters (e.g., frequency, waveform shape, waveform amplitude) of drive signals appearing at the drive signal outputs 210a, 210b, 210c. In certain forms and as discussed below, the logic device 216, in conjunction with a processor (e.g., a digital signal processor discussed below), may implement a number of digital signal processing (DSP)-based and/or other control algorithms to control parameters of the drive signals output by the generator 200.
Power may be supplied to a power rail of the power amplifier 212 by a switch-mode regulator 220, e.g., power converter. In certain forms the switch-mode regulator 220 may comprise an adjustable buck regulator, for example. The non-isolated stage 204 may further comprise a first processor 222, which in one form may comprise a DSP processor such as an Analog Devices ADSP-21469 SHARC DSP, available from Analog Devices, Norwood, Mass., for example, although in various forms any suitable processor may be employed. In certain forms the DSP processor 222 may control operation of the switch-mode regulator 220 responsive to voltage feedback data received from the power amplifier 212 by the DSP processor 222 via an analog-to-digital converter (ADC) circuit 224. In one form, for example, the DSP processor 222 may receive as input, via the ADC circuit 224, the waveform envelope of a signal (e.g., an RF signal) being amplified by the power amplifier 212. The DSP processor 222 may then control the switch-mode regulator 220 (e.g., via a pulse-width modulated (PWM) output) such that the rail voltage supplied to the power amplifier 212 tracks the waveform envelope of the amplified signal. By dynamically modulating the rail voltage of the power amplifier 212 based on the waveform envelope, the efficiency of the power amplifier 212 may be significantly improved relative to a fixed rail voltage amplifier schemes.
In certain forms, the logic device 216, in conjunction with the DSP processor 222, may implement a digital synthesis circuit such as a DDS (see e.g.,
The non-isolated stage 204 may further comprise a first ADC circuit 226 and a second ADC circuit 228 coupled to the output of the power transformer 206 via respective isolation transformers 230, 232 for respectively sampling the voltage and current of drive signals output by the generator 200. In certain forms, the ADC circuits 226, 228 may be configured to sample at high speeds (e.g., 80 mega samples per second [MSPS]) to enable oversampling of the drive signals. In one form, for example, the sampling speed of the ADC circuits 226, 228 may enable approximately 200× (depending on frequency) oversampling of the drive signals. In certain forms, the sampling operations of the ADC circuit 226, 228 may be performed by a single ADC circuit receiving input voltage and current signals via a two-way multiplexer. The use of high-speed sampling in forms of the generator 200 may enable, among other things, calculation of the complex current flowing through the motional branch (which may be used in certain forms to implement DDS-based waveform shape control described above), accurate digital filtering of the sampled signals, and calculation of real power consumption with a high degree of precision. Voltage and current feedback data output by the ADC circuits 226, 228 may be received and processed (e.g., first-in-first-out [FIFO] buffer, multiplexer, etc.) by the logic device 216 and stored in data memory for subsequent retrieval by, for example, the DSP processor 222. As noted above, voltage and current feedback data may be used as input to an algorithm for pre-distorting or modifying LUT waveform samples on a dynamic and ongoing basis. In certain forms, this may require each stored voltage and current feedback data pair to be indexed based on, or otherwise associated with, a corresponding LUT sample that was output by the logic device 216 when the voltage and current feedback data pair was acquired. Synchronization of the LUT samples and the voltage and current feedback data in this manner contributes to the correct timing and stability of the pre-distortion algorithm.
In certain forms, the voltage and current feedback data may be used to control the frequency and/or amplitude (e.g., current amplitude) of the drive signals. In one form, for example, voltage and current feedback data may be used to determine impedance phase. The frequency of the drive signal may then be controlled to minimize or reduce the difference between the determined impedance phase and an impedance phase setpoint (e.g., 0°), thereby minimizing or reducing the effects of harmonic distortion and correspondingly enhancing impedance phase measurement accuracy. The determination of phase impedance and a frequency control signal may be implemented in the DSP processor 222, for example, with the frequency control signal being supplied as input to a DDS control algorithm implemented by the logic device 216.
In another form, for example, the current feedback data may be monitored in order to maintain the current amplitude of the drive signal at a current amplitude setpoint. The current amplitude setpoint may be specified directly or determined indirectly based on specified voltage amplitude and power setpoints. In certain forms, control of the current amplitude may be implemented by control algorithm, such as, for example, a proportional-integral-derivative (PID) control algorithm, in the DSP processor 222. Variables controlled by the control algorithm to suitably control the current amplitude of the drive signal may include, for example, the scaling of the LUT waveform samples stored in the logic device 216 and/or the full-scale output voltage of the DAC circuit 218 (which supplies the input to the power amplifier 212) via a DAC circuit 234.
The non-isolated stage 204 may further comprise a second processor 236 for providing, among other things user interface (UI) functionality. In one form, the UI processor 236 may comprise an Atmel AT91SAM9263 processor having an ARM 926EJ-S core, available from Atmel Corporation, San Jose, Calif., for example. Examples of UI functionality supported by the UI processor 236 may include audible and visual user feedback, communication with peripheral devices (e.g., via a Universal Serial Bus [USB] interface), communication with the foot switch 130, communication with an input device 110 (e.g., a touch screen display) and communication with an output device 112 (e.g., a speaker), as shown in
In certain forms, both the DSP processor 222 and the UI processor 236, for example, may determine and monitor the operating state of the generator 200. For the DSP processor 222, the operating state of the generator 200 may dictate, for example, which control and/or diagnostic processes are implemented by the DSP processor 222. For the UI processor 236, the operating state of the generator 200 may dictate, for example, which elements of a user interface (e.g., display screens, sounds) are presented to a user. The respective DSP and UI processors 222, 236 may independently maintain the current operating state of the generator 200 and recognize and evaluate possible transitions out of the current operating state. The DSP processor 222 may function as the master in this relationship and determine when transitions between operating states are to occur. The UI processor 236 may be aware of valid transitions between operating states and may confirm if a particular transition is appropriate. For example, when the DSP processor 222 instructs the UI processor 236 to transition to a specific state, the UI processor 236 may verify that requested transition is valid. In the event that a requested transition between states is determined to be invalid by the UI processor 236, the UI processor 236 may cause the generator 200 to enter a failure mode.
The non-isolated stage 204 may further comprise a controller 238 for monitoring input devices 110 (e.g., a capacitive touch sensor used for turning the generator 200 on and off, a capacitive touch screen). In certain forms, the controller 238 may comprise at least one processor and/or other controller device in communication with the UI processor 236. In one form, for example, the controller 238 may comprise a processor (e.g., a Mega168 8-bit controller available from Atmel) configured to monitor user input provided via one or more capacitive touch sensors. In one form, the controller 238 may comprise a touch screen controller (e.g., a QT5480 touch screen controller available from Atmel) to control and manage the acquisition of touch data from a capacitive touch screen.
In certain forms, when the generator 200 is in a “power off” state, the controller 238 may continue to receive operating power (e.g., via a line from a power supply of the generator 200, such as the power supply 254 discussed below). In this way, the controller 196 may continue to monitor an input device 110 (e.g., a capacitive touch sensor located on a front panel of the generator 200) for turning the generator 200 on and off. When the generator 200 is in the power off state, the controller 238 may wake the power supply (e.g., enable operation of one or more DC/DC voltage converters 256 of the power supply 254) if activation of the “on/off” input device 110 by a user is detected. The controller 238 may therefore initiate a sequence for transitioning the generator 200 to a “power on” state. Conversely, the controller 238 may initiate a sequence for transitioning the generator 200 to the power off state if activation of the “on/off” input device 110 is detected when the generator 200 is in the power on state. In certain forms, for example, the controller 238 may report activation of the “on/off” input device 110 to the UI processor 236, which in turn implements the necessary process sequence for transitioning the generator 200 to the power off state. In such forms, the controller 196 may have no independent ability for causing the removal of power from the generator 200 after its power on state has been established.
In certain forms, the controller 238 may cause the generator 200 to provide audible or other sensory feedback for alerting the user that a power on or power off sequence has been initiated. Such an alert may be provided at the beginning of a power on or power off sequence and prior to the commencement of other processes associated with the sequence.
In certain forms, the isolated stage 202 may comprise an instrument interface circuit 240 to, for example, provide a communication interface between a control circuit of a surgical instrument (e.g., a control circuit comprising handpiece switches) and components of the non-isolated stage 204, such as, for example, the logic device 216, the DSP processor 222 and/or the UI processor 236. The instrument interface circuit 240 may exchange information with components of the non-isolated stage 204 via a communication link that maintains a suitable degree of electrical isolation between the isolated and non-isolated stages 202, 204, such as, for example, an infrared (IR)-based communication link. Power may be supplied to the instrument interface circuit 240 using, for example, a low-dropout voltage regulator powered by an isolation transformer driven from the non-isolated stage 204.
In one form, the instrument interface circuit 240 may comprise a logic circuit 242 (e.g., logic circuit, programmable logic circuit, PGA, FPGA, PLD) in communication with a signal conditioning circuit 244. The signal conditioning circuit 244 may be configured to receive a periodic signal from the logic circuit 242 (e.g., a 2 kHz square wave) to generate a bipolar interrogation signal having an identical frequency. The interrogation signal may be generated, for example, using a bipolar current source fed by a differential amplifier. The interrogation signal may be communicated to a surgical instrument control circuit (e.g., by using a conductive pair in a cable that connects the generator 200 to the surgical instrument) and monitored to determine a state or configuration of the control circuit. The control circuit may comprise a number of switches, resistors and/or diodes to modify one or more characteristics (e.g., amplitude, rectification) of the interrogation signal such that a state or configuration of the control circuit is uniquely discernable based on the one or more characteristics. In one form, for example, the signal conditioning circuit 244 may comprise an ADC circuit for generating samples of a voltage signal appearing across inputs of the control circuit resulting from passage of interrogation signal therethrough. The logic circuit 242 (or a component of the non-isolated stage 204) may then determine the state or configuration of the control circuit based on the ADC circuit samples.
In one form, the instrument interface circuit 240 may comprise a first data circuit interface 246 to enable information exchange between the logic circuit 242 (or other element of the instrument interface circuit 240) and a first data circuit disposed in or otherwise associated with a surgical instrument. In certain forms, for example, a first data circuit 136 (
In certain forms, the first data circuit 136 *
As discussed previously, a surgical instrument may be detachable from a handpiece (e.g., the multifunction surgical instrument 108 may be detachable from the handpiece 109) to promote instrument interchangeability and/or disposability. In such cases, conventional generators may be limited in their ability to recognize particular instrument configurations being used and to optimize control and diagnostic processes accordingly. The addition of readable data circuits to surgical instruments to address this issue is problematic from a compatibility standpoint, however. For example, designing a surgical instrument to remain backwardly compatible with generators that lack the requisite data reading functionality may be impractical due to, for example, differing signal schemes, design complexity, and cost. Forms of instruments discussed herein address these concerns by using data circuits that may be implemented in existing surgical instruments economically and with minimal design changes to preserve compatibility of the surgical instruments with current generator platforms.
Additionally, forms of the generator 200 may enable communication with instrument-based data circuits. For example, the generator 200 may be configured to communicate with a second data circuit 138 (
In some forms, the second data circuit 138 (
In certain forms, the second data circuit and the second data circuit interface 248 may be configured such that communication between the logic circuit 242 and the second data circuit can be effected without the need to provide additional conductors for this purpose (e.g., dedicated conductors of a cable connecting a handpiece to the generator 200). In one form, for example, information may be communicated to and from the second data circuit using a 1-wire bus communication scheme implemented on existing cabling, such as one of the conductors used transmit interrogation signals from the signal conditioning circuit 244 to a control circuit in a handpiece. In this way, design changes or modifications to the surgical instrument that might otherwise be necessary are minimized or reduced. Moreover, because different types of communications implemented over a common physical channel can be frequency-band separated, the presence of a second data circuit may be “invisible” to generators that do not have the requisite data reading functionality, thus enabling backward compatibility of the surgical instrument.
In certain forms, the isolated stage 202 may comprise at least one blocking capacitor 250-1 connected to the drive signal output 210b to prevent passage of DC current to a patient. A single blocking capacitor may be required to comply with medical regulations or standards, for example. While failure in single-capacitor designs is relatively uncommon, such failure may nonetheless have negative consequences. In one form, a second blocking capacitor 250-2 may be provided in series with the blocking capacitor 250-1, with current leakage from a point between the blocking capacitors 250-1, 250-2 being monitored by, for example, an ADC circuit 252 for sampling a voltage induced by leakage current. The samples may be received by the logic circuit 242, for example. Based changes in the leakage current (as indicated by the voltage samples in the form of
In certain forms, the non-isolated stage 204 may comprise a power supply 254 for delivering DC power at a suitable voltage and current. The power supply may comprise, for example, a 400 W power supply for delivering a 48 VDC system voltage. The power supply 254 may further comprise one or more DC/DC voltage converters 256 for receiving the output of the power supply to generate DC outputs at the voltages and currents required by the various components of the generator 200. As discussed above in connection with the controller 238, one or more of the DC/DC voltage converters 256 may receive an input from the controller 238 when activation of the “on/off” input device 110 by a user is detected by the controller 238 to enable operation of, or wake, the DC/DC voltage converters 256.
In one form, the generator 300 drive system 302 may comprise one or more embedded applications implemented as firmware, software, hardware, or any combination thereof. The generator 300 drive system 302 may comprise various executable modules such as software, programs, data, drivers, application program interfaces (APIs), and so forth. The firmware may be stored in nonvolatile memory (NVM), such as in bit-masked read-only memory (ROM) or flash memory. In various implementations, storing the firmware in ROM may preserve flash memory. The NVM may comprise other types of memory including, for example, programmable ROM (PROM), erasable programmable ROM (EPROM), EEPROM, or battery backed random-access memory (RAM) such as dynamic RAM (DRAM), Double-Data-Rate DRAM (DDRAM), and/or synchronous DRAM (SDRAM).
In one form, the generator 300 drive system 302 comprises a hardware component implemented as a processor 308 for executing program instructions for monitoring various measurable characteristics of the ultrasonic surgical instrument 104 (
In one form, under control of one or more software program routines, the processor 308 executes the methods in accordance with the described forms to generate an electrical signal output waveform comprising current (I), voltage (V), and/or frequency (f) for various time intervals or periods (T). The stepwise waveforms of the drive signals may be generated by forming a piecewise linear combination of constant functions over a plurality of time intervals created by stepping the generator 300 drive signals, e.g., output drive current (I), voltage (V), and/or frequency (f). The time intervals or periods (T) may be predetermined (e.g., fixed and/or programmed by the user) or may be variable. Variable time intervals may be defined by setting the drive signal to a first value and maintaining the drive signal at that value until a change is detected in a monitored characteristic. Examples of monitored characteristics may comprise, for example, transducer impedance, tissue impedance, tissue heating, tissue transection, tissue coagulation, and the like. The ultrasonic drive signals generated by the generator 300 include, without limitation, ultrasonic drive signals capable of exciting the ultrasonic transducer 306 in various vibratory modes such as, for example, the primary longitudinal mode and harmonics thereof as well flexural and torsional vibratory modes.
In one form, the executable modules comprise one or more algorithm(s) 310 stored in memory that when executed causes the processor 308 to generate an electrical signal output waveform comprising current (I), voltage (V), and/or frequency (f) for various time intervals or periods (T). The stepwise waveforms of the drive signals may be generated by forming a piecewise linear combination of constant functions over two or more time intervals created by stepping the output drive current (I), voltage (V), and/or frequency (f) of the generator 300. The drive signals may be generated either for predetermined fixed time intervals or periods (T) of time or variable time intervals or periods of time in accordance with the one or more algorithm(s) 310. Under control of the processor 308, the generator 100 outputs (e.g., increases or decreases) the current (I), voltage (V), and/or frequency (f) up or down at a particular resolution for a predetermined period (T) or until a predetermined condition is detected, such as a change in a monitored characteristic (e.g., transducer impedance, tissue impedance). The steps can change in programmed increments or decrements. If other steps are desired, the generator 300 can increase or decrease the step adaptively based on measured system characteristics.
In operation, the user can program the operation of the generator 300 using the input device 312 located on the front panel of the generator 300 console. The input device 312 may comprise any suitable device that generates signals 314 that can be applied to the processor 308 to control the operation of the generator 300. In various forms, the input device 312 includes buttons, switches, thumbwheels, keyboard, keypad, touch screen monitor, pointing device, remote connection to a general purpose or dedicated computer. In other forms, the input device 312 may comprise a suitable user interface. Accordingly, by way of the input device 312, the user can set or program the current (I), voltage (V), frequency (f), and/or period (T) for programming the output of the generator 300. The processor 308 then displays the selected power level by sending a signal on line 316 to an output indicator 318.
In various forms, the output indicator 318 may provide visual, audible, and/or tactile feedback to the surgeon to indicate the status of a surgical procedure, such as, for example, when tissue cutting and coagulating is complete based on a measured characteristic of the ultrasonic surgical instrument 104, e.g., transducer impedance, tissue impedance, or other measurements as subsequently described. By way of example, and not limitation, visual feedback comprises any type of visual indication device including incandescent lamps or LEDs, graphical user interface, display, analog indicator, digital indicator, bar graph display, digital alphanumeric display. By way of example, and not limitation, audible feedback comprises any type of buzzer, computer generated tone, computerized speech, voice user interface (VUI) to interact with computers through a voice/speech platform. By way of example, and not limitation, tactile feedback comprises any type of vibratory feedback provided through an instrument housing handle assembly.
In one form, the processor 308 may be configured or programmed to generate a digital current signal 320 and a digital frequency signal 322. These digital signals 320, 322 are applied to a digital synthesis circuit such as the DDS circuit 324 (see e.g.,
In one form, the generator 300 comprises one or more measurement modules or components that may be configured to monitor measurable characteristics of the ultrasonic instrument 104 (
The generator 400 comprises a tissue impedance module 442. The drive system 402 is configured to generate electrical drive signal 404 to drive the ultrasonic transducer 406. In one aspect, the tissue impedance module 442 may be configured to measure the impedance Zt of tissue grasped between the blade 440 and the clamp arm assembly 444. The tissue impedance module 442 comprises an RF oscillator 446, an RF voltage sensing circuit 448, and an RF current sensing circuit 450. The RF voltage and RF current sensing circuits 448, 450 respond to the RF voltage Vrf applied to the blade 440 electrode and the RF current Irf flowing through the blade 440 electrode, the tissue, and the conductive portion of the clamp arm assembly 444. The sensed voltage Vrf and current Irf are converted to digital form by the ADC circuit 436 via the analog multiplexer 434. The processor 408 receives the digital output 438 of the ADC circuit 436 and determines the tissue impedance Zt by calculating the ratio of the RF voltage Vrf to current Irf measured by the RF voltage sense circuit 448 and the RF current sense circuit 450. In one aspect, the transection of the inner muscle layer and the tissue may be detected by sensing the tissue impedance Zt. Accordingly, detection of the tissue impedance Zt may be integrated with an automated process for separating the inner muscle layer from the outer adventitia layer prior to transecting the tissue without causing a significant amount of heating, which normally occurs at resonance.
In one form, the RF voltage Vrf applied to the blade 440 electrode and the RF current Irf flowing through the blade 440 electrode, the tissue, and the conductive portion of the clamp arm assembly 451 are suitable for vessel sealing and/or dissecting. Thus, the RF power output of the generator 400 can be selected for non-therapeutic functions such as tissue impedance measurements as well as therapeutic functions such as vessel sealing and/or dissection. It will be appreciated, that in the context of the present disclosure, the ultrasonic and the RF electrosurgical energies can be supplied by the generator either individually or simultaneously.
In various forms, feedback is provided by the output indicator 418 shown in
In one form, the processor 408 may be configured or programmed to generate a digital current signal 420 and a digital frequency signal 422. These digital signals 420, 422 are applied to a digital synthesis circuit such as the DDS circuit 424 (see e.g.,
In one form, the generator 400 comprises one or more measurement modules or components that may be configured to monitor measurable characteristics of the ultrasonic instrument 104 (
With reference to
A first voltage sensing circuit 512 is coupled across the terminals labeled ENERGY1 and the RETURN path to measure the output voltage therebetween. A second voltage sensing circuit 524 is coupled across the terminals labeled ENERGY2 and the RETURN path to measure the output voltage therebetween. A current sensing circuit 514 is disposed in series with the RETURN leg of the secondary side of the power transformer 508 as shown to measure the output current for either energy modality. If different return paths are provided for each energy modality, then a separate current sensing circuit should be provided in each return leg. The outputs of the first and second voltage sensing circuits 512, 524 are provided to respective isolation transformers 516, 522 and the output of the current sensing circuit 514 is provided to another isolation transformer 518. The outputs of the isolation transformers 516, 518, 522 in the on the primary side of the power transformer 508 (non-patient-isolated side) are provided to a one or more ADC circuit 526. The digitized output of the ADC circuit 526 is provided to the processor 502 for further processing and computation. The output voltages and output current feedback information can be employed to adjust the output voltage and current provided to the surgical instrument and to compute output impedance, among other parameters. Input/output communications between the processor 502 and patient isolated circuits is provided through an interface circuit 520. Sensors also may be in electrical communication with the processor 502 by way of the interface circuit 520.
In one aspect, the impedance may be determined by the processor 502 by dividing the output of either the first voltage sensing circuit 512 coupled across the terminals labeled ENERGY1/RETURN or the second voltage sensing circuit 524 coupled across the terminals labeled ENERGY2/RETURN by the output of the current sensing circuit 514 disposed in series with the RETURN leg of the secondary side of the power transformer 508. The outputs of the first and second voltage sensing circuits 512, 524 are provided to separate isolations transformers 516, 522 and the output of the current sensing circuit 514 is provided to another isolation transformer 516. The digitized voltage and current sensing measurements from the ADC circuit 526 are provided the processor 502 for computing impedance. As an example, the first energy modality ENERGY1 may be ultrasonic energy and the second energy modality ENERGY2 may be RF energy. Nevertheless, in addition to ultrasonic and bipolar or monopolar RF energy modalities, other energy modalities include irreversible and/or reversible electroporation and/or microwave energy, among others. Also, although the example illustrated in
As shown in
In other aspects, the generators 100, 200, 300, 400, 500 described in connection with
As shown in
The switching mechanism 1023 is configured to receive the combined energy modalities power output 1005 from the generator 1003 and it may be provided to the energy storage device 1025, surgical instrument 9007, and/or surgical instrument 9008. The device power monitoring component 1031 is coupled to the channels for the energy storage device 1025, surgical instrument 9007, surgical instrument 9008, and may monitor where power is flowing. The control circuit 1019 comprises communication interface 1033 coupled to the HSW serial interface 1011 and an HP serial interface 1013 of the generator 1003. The control circuit 1019 is also coupled to the storage control 1027, storage monitoring component 1029, and device power monitoring component 1031 of the energy storage circuit 1071.
The control circuit 1019 further comprises a serial master interface 1035 that is coupled to HSW #1 circuit 1037 and HSW #2 circuit 1038, includes generation and ADC circuit, a form of memory (non volatile or flash) 1039, along with a method for detecting the presence of an attached instrument (Presence) #1 circuit 1041 and Presence #2 circuit 1042, which includes a voltage or current source and ADC circuit. The serial master interface 1035 also includes HSW NVM bypass channels, which couple the serial master interface 1035 to the outputs of the HSW #1 circuit 1037 and the HSW #2 circuit 1038, respectively. The HSW #1 circuit 1037 and HSW #2 circuit 1038 are coupled to the HSW 1-wire serial protocol interfaces 9013, 9014 of the surgical instruments 9007, 9008, respectively. The serial master interface 1035 further includes HP serial channels that are coupled to the HP 1-wire serial protocol interfaces 9015, 9016 of the surgical instruments 9007, 9008, respectively. Further, Presence #1 and Presence #2 circuits 1041, 1042 are coupled to the presence interfaces 9017, 9018 of the surgical instruments 9007, 9008, respectively.
The system 1001 allows the control circuit 1019, such as an FPGA, to communicate with more surgical instruments using adapter 1015, which acts as an expansion adapter device. According to various aspects, the adapter 1015 expands the Input/Output (I/O) capability of the generator 1003 control. The adapter 1015 may function as an extension of the central processing unit that allows commands to be transmitted over a bus between the adapter 1015 and the generator 1003 and unpacks the commands and use them to bit-bang over interfaces or to control connected analog circuit. The adapter 1015 also allows for reading in ADC values from connected surgical instruments 9007, 9008 and relay this information to the generator control and the generator control would then control the two surgical instruments 9007, 9008. According to various aspects, the generator 1003 may control the surgical instruments 9007, 9008 as two separate state machines and may store the data.
Existing interfaces (the HSW serial interface 1011 and the HP serial interface 1013 lines from generator 1003) may be used in a two-wire communication protocol that enables the generator 1003 control to communicate with multiple surgical instruments connected to a dual port interface, similar to the topology of a universal serial bus (USB) hub.
This allows interfacing with two separate surgical instruments simultaneously. The system 1001 may be able to generate and read hand switch waveforms and be able to handle incoming HP serial buses. It would also monitor two separate presence elements in the surgical instruments 9007, 9008. In one aspect, the system 1001 may include a unique presence element and may have its own NVM.
Further, according to various aspects, the control circuit 1019 may be controlled by the generator 1003. The communication between the adapter 1015 and connected surgical instruments 9007, 9008 may be relayed to generator control. The generator 1003 would control the waveform generation circuit connected to the adapter 1015 to simultaneously generate HSW signals for surgical instruments 9007, 9008.
The system 1001 may allow surgical instrument activity that can be simultaneously detected/monitored for two surgical instruments, even during activation. If upgradeable, the adapter 1015 would be capable of handling new surgical instrument communications protocols. Further, fast switching between surgical instruments may be accomplished.
The adapter 1115 comprises an energy storage circuit 1117, control circuit 1119, an adapter memory 1121 (e.g., a NVM such as an EEPROM), a serial programmable input/output (PIO) integrated circuit 1133, a HSW switching mechanism 1135, a HP switching mechanism 1137, a presence switching mechanism 1139, and a generic adapter 1141. In one aspect, the serial PIO integrated circuit 1133 may be an addressable switch. The energy storage circuit 1117 comprises a switching mechanism 1123, energy storage device 1125, storage control component 1127, storage monitoring component 1129, and a device power monitoring component 1131. The control circuit 1119 may comprise a processor, FPGA, CPLD, PLD, microcontroller, DSP, and/or an ASIC, for example. According to the aspect of
The switching mechanism 1123 is configured to receive the combined energy modalities energy power output 1105 from the generator 1103 and it may be provided to the energy storage device 1125, surgical instrument 9007, and/or surgical instrument 9008. The device power monitoring component 1131 is coupled to the channels for the energy storage device 1125, surgical instrument 9007, surgical instrument 9008, and may monitor where power is flowing.
The control circuit 1119 is coupled to the serial PIO integrated circuit 1133 and the serial PIO integrated circuit 1133 is coupled to the HP serial interface 1113 of the generator 1103. The control circuit 1119 may receive information regarding charger status flags and switching controls from the serial PIO integrated circuit 1133. Further, the control circuit 1119 is coupled to the HSW switching mechanism 1135, the HP switching mechanism 1137, and the presence switching mechanism 1139. According to the aspect of
The HSW switching mechanism 1135, the HP switching mechanism 1137, and the presence switching mechanism 1139 are coupled to the HSW serial interface 1111, the HP serial interface 1113, and the presence interface 1109 of generator 1103, respectively. Further, the HSW switching mechanism 1135, the HP switching mechanism 1137, and the presence switching mechanism 1139 are coupled to the HSW 1-wire serial protocol interfaces 9013, 9014, the HP 1-wire serial protocol interfaces 9015, 9016, and the presence interfaces 9017, 9018 of the surgical instruments 9007, 9008, respectively. Further, the presence switching mechanism 1139 is coupled to the generic adapter 1141.
The generator 1103 switches between monitoring the surgical instruments 9007, 9008. According to various aspects, this switching may require the generator 1103 control to keep track of surgical instruments 9007, 9008 and run two separate state machines. The control circuit 1119 will need to remember which surgical instruments are connected, so that it can output an appropriate waveform to the ports where appropriate. The generator 1103 may generate/monitor hand switch signals, as well as communicating with serial NVM devices, such as the adapter memory 1121. The generator 1103 may maintain constant communication with the activating surgical instrument for the duration of the activation.
System 1101 also allows for a generic adapter presence element. When first plugged in or powered on, the adapter 1115 would present this adapter resistance to the generator 1103. The generator 1103 may then relay commands to the adapter 1115 to switch between the different presence elements corresponding to the different surgical instruments 9007, 9008 connected to it. Accordingly, the generator 1103 is able to use its existing presence resistance circuit. The NVM adapter memory 1121 exists on the adapter 1115 for additional identification of the adapter and to provide a level of security. In addition, the adapter 1115 has a serial I/O device, i.e., serial PIO integrated circuit 1133. The serial PIO integrated circuit 1133 provides a communication link between the generator 1103 and the adapter 1115.
It may be possible to communicate over the HP serial bus using serial communications to HP NVMs and UART style communication to the control circuit 1119. According to one aspect, if SLOW serial communication is used (i.e. not overdrive) and a high speed serial protocol is used, system 1101 may need to ensure that the communications protocol does not generate a signal that looked like a serial reset pulse. This would allow better generator 1103 to adapter 1115 communications and faster switching times between surgical instruments 9007, 9008.
The system 1101 uses generator communications protocol and analog circuit and allows the generator to accomplish decision making. It is a simple and efficient solution that uses a small number of circuit devices.
The control circuit 1219 is coupled to the HSW serial interface 1211 of the generator 1203 while the serial PIO integrated circuit 1233 is coupled to the HP serial interface 1213 as is the HP switching mechanism 1221. Further, the control circuit 1119 is coupled to the HSW #1 circuit 1231 and the HSW #2 circuit 1271. The control circuit 1119 may comprise a processor, FPGA, CPLD, PLD, microcontroller, and/or ASIC, for example. In the example shown in
The switching mechanism 1223 is configured to receive the combined RF/ultrasonic energy modalities output power 1205 from the generator 1203 and it may be provided to the energy storage circuit 1225 or the switching mechanism 1235. The control circuit 1219 is also coupled to the storage control 1227 and energy storage monitoring 1229 of the energy storage circuit 1217. The switching mechanism 1235 may provide the power output received from the switching mechanism 1223 to surgical instrument 9007, and/or surgical instrument 9008. The instrument power monitoring 1237 is coupled to the channels for the power output to the surgical instrument 9007 and surgical instrument 9008. The instrument power monitoring 1237 also may ensure that the switching mechanism 1235 is delivering power to correct location.
The HSW #1 circuit 1231 and the HSW #2 circuit 1271 are coupled to the HSW 1-wire serial protocol interfaces 9013, 9014 of the surgical instruments 9007, 9008, respectively. The HP switching mechanism 1221 is coupled to the HP serial interface 1213 of the generator 1203 and to the HP 1-wire serial protocol interfaces 9015, 9016 of the surgical instruments 9007, 9008, respectively. Further, the presence switching mechanism 1239 is coupled to the presence interface 1209 of the generator 1203 and to the presence interfaces 9017, 9018 of the surgical instruments 9007, 9008, respectively. Further, Presence Switching mechanism is coupled to the unique presence 1241. In one aspect, different instrument presence elements may be switched on an on-demand basis using serial I/O or an adapter micro protocol.
A first communications protocol will be used to communicate to the control circuit 1219 on the adapter 1215. The generator 1203 also may have the ability to monitor surgical instruments 9007, 9008 at once. The adapter 1215 may comprise circuit to provide HSW signal generation (e.g., in HSW #1 circuit 1231 and HSW #2 circuit 1271) along with ADC circuits to interpret this data. The adapter 1215 may modulate two surgical instrument signals into at least a first waveform and may have the ability to read in the first and second waveforms. In various aspects, the second waveforms may be interpreted and translated into the format of the first waveforms. Further, the first protocol has the ability to send 12 bits at 615 bits/sec.
The control circuit 1219 may take the HSW data from surgical instruments 9007, 9008 and modulate it into a first protocol. There are a few ways of doing this, but it may mean that surgical instruments 9007, 9008 may comprise a first protocol functionality. The system 1201 could communicate 4-6 buttons from the surgical instrument 9007 and 4-6 buttons from the surgical instrument 9008 in the first protocol frame. Alternatively, the system 1201 could use some form of addressing to access the surgical instruments 9007, 9008. The control circuit 1219 may have the ability to address separate devices by having the generator 1203 send the control circuit 1219 different addresses split into two different address spaces, one for surgical instrument 9007 and one for surgical instrument 9008.
The HP communications may involve some form of switch that could either be controlled via a serial I/O device or through the control circuit 1219 via a first protocol style communication interface from the generator 1203. In one aspect, energy storage monitoring 1229 and switching between surgical instruments 9007, 9008 and charging states could be handled in this manner as well. Certain first protocol addresses could be assigned to the data from the energy storage circuit 1225 and to the surgical instruments 9007, 9008 themselves. Presence elements could also be switched in with this format. Further, in one aspect, the control circuit 1219 may translate frames into a separate format, which may mean that the control circuit 1219 might need to make some decisions on whether button presses on surgical instruments 9007, 9008 are valid or not. The system 1201 would, however, allow the generator 1203 to fully monitor the surgical instruments 9007, 9008 at the same time time-slicing or handling a new communications protocol on the HSW serial interface 1211 of the generator 1203. The system 1201 uses generator communications to simultaneously detect the activity of two surgical instruments, even during activation.
The surgical instruments described herein may be configured to deliver energy from any of the generators 100, 200, 300, 400, 500, 9001, 1003, 1103, 1203 discussed herein. The energy may be dynamically changed based on the type of tissue being treated by an end effector of a surgical instrument and various characteristics of the tissue. For conciseness and clarity of disclosure any of the generators 100, 200, 300, 400, 500, 9001, 1003, 1103, 1203 described hereinabove will be described hereinbelow as generator 100. It will be appreciated that in this context the generator 100 may comprise functional circuits and algorithms described in connection with the generators 200, 300, 400, 500, 9001, 1003, 1103, 1203, taken alone or in combination, as may be appropriate without departing from the scope of the present disclosure. Accordingly, the reader is directed to the description of the functional blocks of the generators 200, 300, 400, 500, 9001, 1003, 1103, 1203, in
In one aspect, the generator 100 is coupled to the combination RF electrosurgical/ultrasonic instrument 108 shown and described in connection with
According to the present disclosure, the generator 100 may be configured to output an analog output signal usually in the form of a sinusoid at some predetermined frequency or wavelength. The output signal may be characterized by a variety of different types, frequencies, and shapes of electrical signal waveforms suitable for effecting a desired therapy to the tissue. Electrical signal waveforms are basically visual representations of the variation of voltage or current along the vertical axis over time along the horizontal axis represent the shape of the waveform as shown in
In one aspect, the generator 100 is configured to generate the electrical signal waveform digitally such that the desired using a predetermined number of phase points stored in a lookup table to digitize the wave shape. The phase points may be stored in a table defined in a memory, a FPGA, or any suitable non-volatile memory.
The waveform signal may be configured to control at least one of an output current, an output voltage, or an output power of an ultrasonic transducer and/or an RF electrode, or multiples thereof (e.g. two or more ultrasonic transducers and/or two or more RF electrodes). Further, where the surgical instrument comprises an ultrasonic components, the waveform signal may be configured to drive at least two vibration modes of an ultrasonic transducer of the at least one surgical instrument. Accordingly, a generator may be configured to provide a waveform signal to at least one surgical instrument wherein the waveform signal corresponds to at least one wave shape of a plurality of wave shapes in a table. Further, the waveform signal provided to the two surgical instruments may comprise two or more wave shapes. The table may comprise information associated with a plurality of wave shapes and the table may be stored within the generator. In one embodiment or example, the table may be a direct digital synthesis table, which may be stored in an FPGA of the generator. The table may be addressed by anyway that is convenient for categorizing wave shapes. According to one embodiment, the table, which may be a direct digital synthesis table, is addressed according to a frequency of the waveform signal. Additionally, the information associated with the plurality of wave shapes may be stored as digital information in the table.
The analog electrical signal waveform may be configured to control at least one of an output current, an output voltage, or an output power of an ultrasonic transducer and/or an RF electrode, or multiples thereof (e.g., two or more ultrasonic transducers and/or two or more RF electrodes). Further, where the surgical instrument comprises ultrasonic components, the analog electrical signal waveform may be configured to drive at least two vibration modes of an ultrasonic transducer of the at least one surgical instrument. Accordingly, the generator 100 may be configured to provide an analog electrical signal waveform to at least one surgical instrument wherein the analog electrical signal waveform corresponds to at least one wave shape of a plurality of wave shapes stored in a lookup table 1304. Further, the analog electrical signal waveform provided to the two surgical instruments may comprise two or more wave shapes. The lookup table 1304 may comprise information associated with a plurality of wave shapes and the lookup table 1304 may be stored either within the generator 100 or the surgical instrument. In one embodiment or example, the lookup table 1304 may be a direct digital synthesis table, which may be stored in an FPGA of the generator 100 or the surgical instrument. The lookup table 1304 may be addressed by anyway that is convenient for categorizing wave shapes. According to one aspect, the lookup table 1304, which may be a direct digital synthesis table, is addressed according to a frequency of the desired analog electrical signal waveform. Additionally, the information associated with the plurality of wave shapes may be stored as digital information in the lookup table 1304.
With the widespread use of digital techniques in instrumentation and communications systems, a digitally-controlled method of generating multiple frequencies from a reference frequency source has evolved and is referred to as direct digital synthesis. The basic architecture is shown in
Because the DDS circuit 1300 is a sampled data system, issues involved in sampling must be considered: quantization noise, aliasing, filtering, etc. For instance, the higher order harmonics of the DAC circuit 1308 output frequencies fold back into the Nyquist bandwidth, making them unfilterable, whereas, the higher order harmonics of the output of phase-locked-loop (PLL) based synthesizers can be filtered. The lookup table 1304 contains signal data for an integral number of cycles. The final output frequency fout can be changed changing the reference clock frequency fc or by reprogramming the PROM.
The DDS circuit 1300 may comprise multiple lookup tables 1304 where each lookup table 1304 stores a waveform represented by a predetermined number of samples, wherein the samples define a predetermined shape of the waveform. Thus multiple waveforms, each having a unique shape, can be stored in multiple lookup tables 1304 to provide different tissue treatments based on instrument settings or tissue feedback. Examples of waveforms include high crest factor RF electrical signal waveforms for surface tissue coagulation, low crest factor RF electrical signal waveform for deeper tissue penetration, and electrical signal waveforms that promote efficient touch-up coagulation. In one aspect, the DDS circuit 1300 can create multiple wave shape lookup tables 1304 and during a tissue treatment procedure (e.g., “on-the-fly” or in virtual real time based on user or sensor inputs) switch between different wave shapes stored in different lookup tables 1304 based on the tissue effect desired and/or tissue feedback. Accordingly, switching between wave shapes can be based on tissue impedance and other factors, for example. In other aspects, the lookup tables 1304 can store electrical signal waveforms shaped to maximize the power delivered into the tissue per cycle (i.e., trapezoidal or square wave). In other aspects, the lookup tables 1304 can store wave shapes synchronized in such way that they make maximizing power delivery by the multifunction surgical instrument 108 when it delivering both RF and ultrasonic drive signals. In yet other aspects, the lookup tables 1304 can store electrical signal waveforms to drive both ultrasonic and RF therapeutic, and/or sub-therapeutic, energy simultaneously while maintaining ultrasonic frequency lock. Custom wave shapes specific to different instruments and their tissue effects can be stored in the non-volatile memory of the generator 100 or in the non-volatile memory (e.g., EEPROM) of the multifunction surgical instrument 108 and be fetched upon connecting the multifunction surgical instrument 108 to the generator 100. An example of an exponentially damped sinusoid, as used in many high crest factor “coagulation” waveforms is shown in
A more flexible and efficient implementation of the DDS circuit 1300 employs a digital circuit called a Numerically Controlled Oscillator (NCO). A block diagram of a more flexible and efficient digital synthesis circuit such as a DDS circuit 1400 is shown in
The DDS circuit 1400 includes a sample clock that generates a clock frequency fc, a phase accumulator 1406, and a lookup table 1410 (e.g., phase to amplitude converter). The content of the phase accumulator 1406 is updated once each clock cycle fc. Each time the phase accumulator 1406 is updated, the digital number, M, stored in the parallel delta phase register 1404 is added to the number in the phase register 1408 by an adder circuit 1416. Assuming that the number in the parallel delta phase register 1404 is 00 . . . 01 and that the initial contents of the phase accumulator 1406 is 00 . . . 00. The phase accumulator 1406 is updated by 00 . . . 01 on each clock cycle. If the phase accumulator 1406 is 32-bits wide, 232 clock cycles (over 4 billion) are required before the phase accumulator 1406 returns to 00 . . . 00, and the cycle repeats.
The truncated output 1418 of the phase accumulator 1406 is provided to a phase-to amplitude converter lookup table 1410 and the output of the lookup table 1410 is coupled to a DAC circuit 1412. The truncated output 1418 of the phase accumulator 1406 serves as the address to a sine (or cosine) lookup table. Each address in the lookup table corresponds to a phase point on the sinewave from 0° to 360°. The lookup table 1410 contains the corresponding digital amplitude information for one complete cycle of a sinewave. The lookup table 1410 therefore maps the phase information from the phase accumulator 1406 into a digital amplitude word, which in turn drives the DAC circuit 1412. The output of the DAC circuit is a first analog signal 1420 and is filtered by a filter 1414. The output of the filter 1414 is a second analog signal 1422, which is provided to a power amplifier 212, 326, 426, 506 (
In one aspect, the electrical signal waveform may be digitized into 1024 (210) phase points, although the wave shape may be digitized is any suitable number of 2n phase points ranging from 256 (28) to 281,474,976,710,656 (248), where n is a positive integer, as shown in TABLE 1. The electrical signal waveform may be expressed as An(θn), where a normalized amplitude An at a point n is represented by a phase angle θn is referred to as a phase point at point n. The number of discrete phase points n determines the tuning resolution of the DDS circuit 1400 (as well as the DDS circuit 1300 shown in
The generator 100 algorithms and digital control circuits scan the addresses in the lookup table 1410, which in turn provides varying digital input values to the DAC circuit 1412 that feeds the filter 1414 and the power amplifier. The addresses may be scanned according to a frequency of interest. Using the lookup table enables generating various types of shapes that can be converted into an analog output signal by the DAC circuit 1412, filtered by the filter 1414, amplified by the power amplifier coupled to the output of the generator 100, and fed to the tissue in the form of RF energy or fed to an ultrasonic transducer and applied to the tissue in the form of ultrasonic vibrations which deliver energy to the tissue in the form of heat. The output of the amplifier can be applied to a single RF electrode, multiple RF electrodes simultaneously, a single ultrasonic transducer, multiple ultrasonic transducers simultaneously, or a combination of RF and ultrasonic transducers, for example. Furthermore, multiple wave shape tables can be created, stored, and applied to tissue from a single generator 100.
With reference back to
For an n-bit phase accumulator 1406 (n generally ranges from 24 to 32 in most DDS systems, but as previously discussed n may be selected from a wide range of options), there are 2n possible phase points. The digital word in the delta phase register, M, represents the amount the phase accumulator is incremented each clock cycle. If fc is the clock frequency, then the frequency of the output sinewave is equal to:
Equation 1 is known as the DDS “tuning equation.” Note that the frequency resolution of the system is equal to fc/2n. For n=32, the resolution is greater than one part in four billion. In one aspect of the DDS circuit 1400, not all of the bits out of the phase accumulator 1406 are passed on to the lookup table 1410, but are truncated, leaving only the first 13 to 15 most significant bits (MSBs), for example. This reduces the size of the lookup table 1410 and does not affect the frequency resolution. The phase truncation only adds a small but acceptable amount of phase noise to the final output.
The electrical signal waveform may be characterized by a current, voltage, or power at a predetermined frequency. Further, where the multifunction surgical instrument 108 comprises ultrasonic components, the electrical signal waveform may be configured to drive at least two vibration modes of an ultrasonic transducer of the at least one multifunction surgical instrument 108. Accordingly, the generator 100 may be configured to provide an electrical signal waveform to at least one multifunction surgical instrument 108 wherein the electrical signal waveform is characterized by a predetermined wave shape stored in the lookup table 1410 (or lookup table 1304
In one aspect, the generator 100 may be configured to provide electrical signal waveforms to at least two surgical instruments simultaneously. The generator 100 also may be configured to provide the electrical signal waveform, which may be characterized two or more wave shapes, via a single output channel of the generator 100 to the two surgical instruments simultaneously. For example, in one aspect the electrical signal waveform comprises a first electrical signal to drive an ultrasonic transducer (e.g., ultrasonic drive signal), a second RF drive signal, and/or a combination of both. In addition, an electrical signal waveform may comprise a plurality of ultrasonic drive signals, a plurality of RF drive signals, and/or a combination of a plurality of ultrasonic and RF drive signals.
In addition, a method of operating the generator 100 according to the present disclosure comprises generating an electrical signal waveform and providing the generated electrical signal waveform to at least one multifunction surgical instrument 108, where generating the electrical signal waveform comprises receiving information associated with the electrical signal waveform from a memory. The generated electrical signal waveform comprises at least one wave shape. Furthermore, providing the generated electrical signal waveform to the at least one multifunction surgical instrument 108 comprises providing the electrical signal waveform to at least two surgical instruments simultaneously.
The generator 100 as described herein may allow for the generation of various types of direct digital synthesis tables. Examples of wave shapes for RF/Electrosurgery signals suitable for treating a variety of tissue generated by the generator 100 include RF signals with a high crest factor (which may be used for surface coagulation in RF mode), a low crest factor RF signals (which may be used for deeper tissue penetration), and waveforms that promote efficient touch-up coagulation. The generator 100 also may generate multiple wave shapes employing a direct digital synthesis lookup table 1410 and, on the fly, can switch between particular wave shapes based on the desired tissue effect. Switching may be based on tissue impedance and/or other factors.
In addition to traditional sine/cosine wave shapes, the generator 100 may be configured to generate wave shape(s) that maximize the power into tissue per cycle (i.e., trapezoidal or square wave). The generator 100 may provide wave shape(s) that are synchronized to maximize the power delivered to the load when driving both RF and ultrasonic signals simultaneously and to maintain ultrasonic frequency lock, provided that the generator 100 includes a circuit topology that enables simultaneously driving RF and ultrasonic signals. Further, custom wave shapes specific to instruments and their tissue effects can be stored in a non-volatile memory (NVM) or an instrument EEPROM and can be fetched upon connecting the multifunction surgical instrument 108 to the generator 100.
The DDS circuit 1400 may comprise multiple lookup tables 1304 where each lookup table 1410 stores a waveform represented by a predetermined number of phase points (also may be referred to as samples), wherein the phase points define a predetermined shape of the waveform. Thus multiple waveforms, each having a unique shape, can be stored in multiple lookup tables 1410 to provide different tissue treatments based on instrument settings or tissue feedback. Examples of waveforms include high crest factor RF electrical signal waveforms for surface tissue coagulation, low crest factor RF electrical signal waveform for deeper tissue penetration, and electrical signal waveforms that promote efficient touch-up coagulation. In one aspect, the DDS circuit 1400 can create multiple wave shape lookup tables 1410 and during a tissue treatment procedure (e.g., “on-the-fly” or in virtual real time based on user or sensor inputs) switch between different wave shapes stored in different lookup tables 1410 based on the tissue effect desired and/or tissue feedback. Accordingly, switching between wave shapes can be based on tissue impedance and other factors, for example. In other aspects, the lookup tables 1410 can store electrical signal waveforms shaped to maximize the power delivered into the tissue per cycle (i.e., trapezoidal or square wave). In other aspects, the lookup tables 1410 can store wave shapes synchronized in such way that they make maximizing power delivery by the multifunction surgical instrument 108 when it delivering both RF and ultrasonic drive signals. In yet other aspects, the lookup tables 1410 can store electrical signal waveforms to drive both ultrasonic and RF therapeutic, and/or sub-therapeutic, energy simultaneously while maintaining ultrasonic frequency lock. Custom wave shapes specific to different instruments and their tissue effects can be stored in the non-volatile memory of the generator 100 or in the non-volatile memory (e.g., EEPROM) of the multifunction surgical instrument 108 and be fetched upon connecting the multifunction surgical instrument 108 to the generator 100. An example of an exponentially damped sinusoid, as used in many high crest factor “coagulation” waveforms is shown in
Examples of waveforms representing energy for delivery from a generator are illustrated in
For example,
For example,
A variety of other techniques can be used for compressing and/or limiting the waveforms of the output signals. It should be noted that the integrity of the ultrasonic output signal 604 (
In various aspects, the generator 100 may be configured to drive multiple surgical instruments 104, 106, 108 simultaneously. Thus the generator 100 may be configured to drive the surgical instruments 104, 106, 108 in multiple vibration modes to achieve a longer active length at the ultrasonic blade 128, 149 and to create different tissue effects.
According to one of the present disclosure, the generator 100 may be configured to provide ultrasonic electrical signal waveforms defining a number of wave shapes to the surgical instrument 104, 108 to provide a desired therapy to tissue at the end effector 122, 125.
In one aspect, the generator 100 may be configured to generate a digital electrical signal waveform such that the desired wave shape can be digitized by a number of phase points or samples which are stored in a lookup table 1304, 1410 defined in volatile or non-volatile memory as discussed above in connection with
In one aspect, the electrical signal waveforms may be defined by an output current, an output voltage, an output power, or frequency suitable to drive the ultrasonic transducer 120 or multiple ultrasonic transducers (e.g. two or more ultrasonic transducers). In the case of the multifunction surgical instrument 108, in addition to driving the ultrasonic transducer 120, the electrical signal waveforms may be defined by an output current, an output voltage, an output power, or frequency suitable to drive the electrodes located in the end effector 125 of the multifunction surgical instrument 108.
Further, in one aspect where the surgical instrument 104, 108 comprises ultrasonic components, the electrical signal waveform may be configured to drive at least two vibration modes of the ultrasonic transducer 120. Accordingly, a generator 100 may be configured to provide a electrical signal waveform to at least one surgical instrument 104, 108 wherein the electrical signal waveform defines at least one wave shape selected out of a plurality of wave shapes stored in the lookup table 1304, 1410. Further, the electrical signal waveform provided to the two surgical instruments 104, 108 may define two or more wave shapes. The lookup table 1304, 1410 may comprise information associated with a plurality of wave shapes and the lookup table 1304, 1410 may be stored in a memory located either in the generator 100 or the surgical instruments 104, 108. In one embodiment or example, the lookup table 1304, 1410 may be a direct digital synthesis table, which may be stored in an FPGA located in the generator 100 or the surgical instruments 104, 108. The lookup table 1304, 1410 may be addressed using any suitable technique for categorizing wave shapes. According to one aspect, the DDS lookup table 1304, 1410 may be addressed according to the frequency of the electrical signal waveform. Additional information associated with the plurality of wave shapes also may be stored as digital information in the DDS lookup table 1304, 1410.
In one aspect, the generator 100 may comprise a DAC circuit 1308, 1412 and a power amplifier 212, 326, 426, 506. The DAC circuit 1308, 1412 is coupled to the power amplifier 212, 326, 426, 506 such that the DAC circuit 1308, 1412 provides the analog electrical signal waveform to a filter 1312, 1414 and the output of the filter 1312, 1414 is provided to the power amplifier 212, 326, 426, 506. The output of the power amplifier 212, 326, 426, 506 is provided to the surgical instrument 104, 108.
Further, in one aspect the generator 100 may be configured to provide the electrical signal waveform to the surgical instruments 104, 106, 108 simultaneously. This may be accomplished through a single output port or channel of the generator 100. The generator 100 also may be configured to provide the electrical signal waveform, which may define two or more wave shapes, via a single output port or channel to the two surgical instruments 104, 108 simultaneously. The analog signal output of the generator 100 may define multiple wave shapes to one or more than one surgical instruments 104, 108. For example, in one aspect, the electrical signal waveform comprises multiple ultrasonic drive signals. In another aspect, the electrical signal waveform comprises multiple ultrasonic drive signals and one or more than one RF signals. Accordingly, an electrical signal waveform output of the generator 100 may comprise multiple ultrasonic drive signals, multiple RF signals, and/or a combination of multiple ultrasonic drive signals and a RF signals.
In one aspect, the generator 100 as described herein may allow for the creation of various types of DDS lookup tables 1304, 1410 within an FPGA located in the generator 100. Some examples of the wave shapes that may be produced by the generator 100 include high crest factor signals (which may be used for surface coagulation), low crest factor signals (which may be used for deeper tissue penetration), and electrical signal waveforms that promote efficient touch-up coagulation. The generator 100 also may create multiple wave shape lookup tables 1304, 1410. The generator 100 can be configured to switch between different electrical signal waveforms for diving ultrasonic transducers 120 during a procedure (e.g., “on-the-fly” or in virtual real time based on user or sensor inputs) based on desired tissue effects or feedback signals associated with the state of the tissue located in the end effector 122, 125. Switching may be based on tissue impedance, tissue temperature, state of coagulation, state of dissection, and/or other factors.
In one aspect, the generator 100 as described herein also may provide, in addition to the traditional sine wave shape, wave shapes that maximizes the power into tissue per cycle (i.e. trapezoidal, square, or triangular wave shapes). It also may provide wave shapes that are synchronized in a manner that would maximize power delivery in the case of an electrical signal waveform comprises RF and ultrasonic signal components to drive ultrasonic and RF therapeutic energy simultaneously while maintaining ultrasonic frequency lock. Further, custom wave shapes specific to various types of surgical instruments 104, 108 and their tissue effects can be stored in a lookup table 1304, 1410 memory located in the generator 100 or the surgical instrument 104, 108, where the memory may be a volatile (RAM) or non-volatile (EEPROM) memory. The wave shape may be fetched from the lookup table 1304, 1410 memory upon connecting the surgical instrument 104, 108 to the generator 100.
With reference to
In one aspect, the method 1500 the power amplifier 212, 326, 426, 506 amplifies the analog signal 1310, 1420 output of the DAC circuit 1308, 1412. In addition, according to the method 1500, the digital processing circuit stores phase points of a digital electrical signal waveform in the lookup table 1304, 1410 defined by the memory circuit. The digital processing circuit stores phase points of multiple digital electrical signal waveforms in corresponding multiple lookup tables 1304, 1410 defined by the memory circuit or other memory circuits. Each of the digital electrical signal waveforms is represented by a predetermined number of phase points. Each of the predetermined number of phase points defines a different wave shape. In accordance with the method 1500, the digital processing circuit receives a feedback signal associated with tissue parameters and modifies the predetermined wave shape according to the feedback signal.
In one aspect, the digital electrical signal waveform represents a RF signal waveform, an ultrasonic signal waveform, or a combination thereof. In one aspect, the digital electrical signal waveform represents a combination of two waveforms having different amplitudes. In one aspect, the digital electrical signal waveform represents a combination of two waveforms having different frequencies. In one aspect, digital electrical signal waveform represents a combination of two waveforms having of different amplitudes. In one aspect, the wave shape is a trapezoid, a sine or cosine wave, a square wave, a triangle wave, or any combinations thereof. In one aspect, the digital electrical signal waveform is a combined RF and ultrasonic signal waveform configured to maintain a predetermined ultrasonic frequency. In one aspect, the first digital electrical signal waveform is a combined RF and ultrasonic waveform configured to deliver maximum power output.
According to various aspects, the electrical signal waveform also may be provided to at least two surgical instruments 104, 106, 108 simultaneously. The surgical instruments 104, 106, 108 may comprise instruments that operate the same modalities or different modalities of surgical treatment techniques. In one aspect, the surgical instruments include at least one ultrasonic surgical instrument and at least one RF surgical instrument.
With reference to
The analog electrical signal waveform may be of a type that provides for the application of a particular treatment modality for a surgical instrument connected to the generator. Accordingly, the analog electrical signal waveform may be a RF waveform, an ultrasonic waveform, or a combination thereof. The analog electrical signal waveform may be a combined RF and ultrasonic waveform and the combined RF and ultrasonic waveform may be configured to maintain a predetermined ultrasonic frequency. In one aspect, the predetermined ultrasonic frequency is a frequency lock based on a surgical instrument 104, 106, 108 connected to the generator 100. In another aspect, the analog electrical signal waveform is a combined RF and ultrasonic waveform and the combined RF and ultrasonic waveform is configured to cause a surgical instrument 104, 106, 108 to deliver a maximum power application of the surgical instrument 104, 106, 108 to tissue engaged with the surgical instrument 104, 106, 108. The maximum power application may be based on the maximum power output of a treatment modality of a surgical instrument 104, 106, 108, such as, for example, an RF modality or an ultrasonic modality. According to further aspects, the analog electrical signal waveform may comprise a high crest factor RF signal, a low crest factor RF signal, or a combination thereof and/or the electrical signal waveform may comprise a sine wave shape, a trapezoidal wave shape, a square wave shape, or a combination thereof. The analog electrical signal waveform may also be configured to provide a desired tissue effect or outcome to tissue engaged by a surgical instrument 104, 106, 108 when the analog electrical signal waveform is received by the surgical instrument 104, 106, 108. In one aspect, the desired tissue effect is at least one of cutting, coagulation, or sealing.
The generator 100 also may be configured to switch between digital or analog versions of multiple electrical signal waveforms. For example, the generator 100 may be configured to switch between a first electrical signal waveform and a second electrical signal waveform based on predetermined criteria, such as, for example, a desired tissue effect and/or feedback from a surgical instrument 104, 106, 108, which may include measured values of a tissue parameter. The tissue parameter may include a tissue type, a tissue amount, a tissue state, or a combination thereof. Accordingly, the method 1600 includes storing a plurality of electrical signal waveforms in a plurality of lookup tables defined in a memory circuit. The electrical signal waveforms are represented by a predetermined number of phase points, wherein the phase points define predetermined wave shapes based on desired tissue effects, tissue parameters, or other parameters associated with the surgical instrument 104, 106, 108 connected to the generator 100.
Additionally, digital phase points of the digital electrical signal waveform may be received by the generator 100 from a surgical instrument 104, 106, 108 connected to the generator 100. The generator 100 may receive the phase points following or upon connection of the surgical instrument 104, 106, 108 to the generator 100. The phase points of the digital electrical signal waveform may be stored in an EEPROM of the surgical instrument 104, 106, 108, which is operable coupled to the generator 100 upon connection of the surgical instrument 104, 106, 108 to the generator 100.
In accordance with the method 1600, the digital processing circuit receives a feedback signal associated with tissue parameters. In one aspect, based on the feedback signal the digital processing circuit switches between the phase point of the first digital electrical signal waveform and the phase point of the second digital electrical signal waveform and the DAC circuit 1308, 1412 converts the retrieved phase point. In another aspect, based on the feedback signal the digital processing circuit synchronizes the phase points of the first and second digital electrical signal waveforms to maximize power delivery per cycle and the DAC circuit 1308, 1412 circuit, the synchronized phase points. In one aspect, the first digital electrical signal waveform represents a RF waveform and the second digital electrical signal waveform represents an ultrasonic signal waveform.
With reference to
In accordance with the method 1700, the digital processing circuit also instructs the DDS circuit 1300, 1400 to store 1708 a second digital electrical signal waveform in a second lookup table 1304, 1410 defined in the memory circuit, or other memory circuit. The second digital electrical signal waveform is represented by a second predetermined number of phase points that are stored in the second lookup table 1304, 1410. The second predetermined number of phase points define a second wave shape. The DDS circuit 1300, 1400 receives 1710 a clock signal. At each clock cycle, the DDS circuit 1300, 1400 retrieves 1712 a phase point from the second lookup table 1304, 1410.
In accordance with the method 1700, the generator 100 or the surgical instrument 104, 106, 108 receives 1714 tissue parameter feedback from sensors in the surgical instrument 104, 106, 108. The feedback may provide information regarding tissue impedance, tissue type, or temperature of the tissue. In other aspects, the feedback may be based on the temperature of the electrode or ultrasonic blade or electrical impedance of the ultrasonic transducer, among other feedback parameters. Based on the tissue parameter feedback, the digital processing circuit determines 1716 whether to switch between the first and second phase points of the first and second electrical signal waveforms or whether to synchronize the first and second phase points of the first and second electrical signal waveforms to maximize power delivery to the tissue per cycle.
If the method 1700 proceeds along the “switch” branch, the digital processing circuit switches 1718 between the phase point of the first digital electrical signal waveform and the phase point of the second digital electrical signal waveform during a tissue treatment procedure (e.g., “on-the-fly” or in virtual real time based on user or sensor inputs). The retrieved phase point of either the first or second electrical signal waveforms is provided to the DAC circuit 1308, 1412. The DAC circuit 1308, 1412 converts 1720 the retrieved phase point of either the first or second electrical signal waveforms to an analog electrical signal. The sample/hold analog output of the DAC circuit 1308, 1412 is filtered by the filter 1312, 1414 and amplified by a power amplifier 212, 326, 426, 506, for example, before the analog electrical signal waveform is provided to the surgical instrument 104, 106, 108.
If the method 1700 proceeds along the “synchronize” branch, the digital processing circuit synchronizes 1722 the phase points of the first and second digital electrical signal waveforms to maximize power delivery per cycle. The synchronized phase points of the first and second digital electrical signal waveforms are provided to the DAC circuit 1308, 1412. The DAC circuit 1308, 1412 converts 1724 the synchronized phase points of the first or second electrical signal waveforms to an analog electrical signal. The analog sample/hold output of the DAC circuit 1308, 1412 is filtered by the filter 1312, 1414 and amplified by a power amplifier 212, 326, 426, 506, for example, before the analog electrical signal waveform is provided to the surgical instrument 104, 106, 108.
In various aspects, the first and second electrical signal waveforms may represent electrical signals having different wave shapes. In one aspect, the first digital electrical signal waveform may represent an RF signal suitable for driving an electrode of an electrosurgical instrument 106 or a multifunction surgical instrument 108 and the second electrical signal waveform may represent an ultrasonic signal for driving an ultrasonic transducer of an ultrasonic instrument 104 or a multifunction surgical instrument 108. The first and second electrical signal waveforms can be delivered separately, simultaneously, individually, or combined in one signal.
Examples of waveforms representing energy for delivery from a generator are illustrated in
For example,
For example,
A variety of other techniques can be used for compressing and/or limiting the waveforms of the output signals. It should be noted that the integrity of the second ultrasonic output signal 1904 (
A variety of techniques can be used for compressing and/or limiting ultrasonic electrical signal waveforms. It should be noted that the integrity of an ultrasonic electrical signal waveform can be more important than the integrity of the RF electrical signal waveform as long as any low frequency components of the RF electrical signal waveform are limited to safe patient levels so as to avoid neuro-muscular stimulation. In another form, the frequency of an RF electrical signal waveform can be changed on a continuous basis in order to manage the peaks of the waveform. Waveform control is important as more complex RF waveforms, are implemented with the system.
The surgical instruments 104, 106, 108 described herein can include features to allow the energy being delivered by the generator 100 to be dynamically changed based on the type of tissue being treated by the end effector 122, 124, 125 of the surgical instrument 104, 106, 108 and various characteristics of the tissue. In one aspect, an algorithm for controlling the power output from a generator 100 that is delivered to the end effector 122, 124, 125 of the surgical instrument 104, 106, 108 can include an input that represents the tissue type to allow the energy profile from the generator 100 to be dynamically changed during the procedure based on the type of tissue being effected by the end effector 122, 124, 125 of the surgical instrument 104, 106, 108.
In accordance with the methods 2000, 2100, the generator 100 comprises a digital processing circuit, a DDS circuit 1300, 1400, a memory circuit defining a lookup table 1304, 1410, and DAC circuit 1308, 1412, as described herein. The digital processing circuit may comprise any digital processing circuit, microprocessor, microcontroller, digital signal processor, logic device comprising combinational logic or sequential logic circuits, or any suitable digital circuit. The memory circuit may be located either in the surgical instrument 104, 108 or the generator 100. In one aspect, the DDS circuit 1300, 1400 is coupled to the digital processing circuit and the memory circuit. In another aspect, the memory circuit is part of the DDS circuit 1300, 1400.
In various aspects, the generator 100 may be configured to drive multiple ultrasonic transducers 120 in one or more ultrasonic surgical instruments 104, 108 simultaneously. Thus the generator 100 may be configured to drive the surgical instruments 104, 108 in multiple vibration modes to achieve a longer active length at the ultrasonic blade 128, 149 and to create different tissue effects.
According to one of the present disclosure, the generator 100 may be configured to provide ultrasonic electrical signal waveforms defining a number of wave shapes to a surgical instrument 104, 108 so that the surgical instrument 104, 108 may apply a desired therapy to tissue at the end effector 122, 125.
In one aspect, the generator 100 may be configured to generate a digital electrical signal waveform such that the desired wave shape can be digitized by a number of phase points or samples which are stored in a lookup table 1304, 1410 defined in volatile or non-volatile memory as discussed above in connection with
In one aspect, the electrical signal waveforms may be defined by an output current, an output voltage, an output power, or frequency suitable to drive the ultrasonic transducer 120 or multiple ultrasonic transducers (e.g. two or more ultrasonic transducers). In the case of the multifunction surgical instrument 108, in addition to driving the ultrasonic transducer 120, the electrical signal waveforms may be defined by an output current, an output voltage, an output power, or frequency suitable to drive the electrodes located in the end effector 125 of the multifunction surgical instrument 108.
Further, in one aspect where the surgical instrument 104, 108 comprises ultrasonic components, the electrical signal waveform may be configured to drive at least two vibration modes of the ultrasonic transducer 120. Accordingly, a generator 100 may be configured to provide a electrical signal waveform to at least one surgical instrument 104, 108 wherein the electrical signal waveform defines at least one wave shape selected out of a plurality of wave shapes stored in the lookup table 1304, 1410. Further, the electrical signal waveform provided to the two surgical instruments 104, 108 may define two or more wave shapes. The lookup table 1304, 1410 may comprise information associated with a plurality of wave shapes and the lookup table 1304, 1410 may be stored in a memory located either in the generator 100 or the surgical instruments 104, 108. In one embodiment or example, the lookup table 1304, 1410 may be a direct digital synthesis table, which may be stored in an FPGA located in the generator 100 or the surgical instruments 104, 108. The lookup table 1304, 1410 may be addressed using any suitable technique for categorizing wave shapes. According to one aspect, the DDS lookup table 1304, 1410 may be addressed according to the frequency of the electrical signal waveform. Additional information associated with the plurality of wave shapes also may be stored as digital information in the DDS lookup table 1304, 1410.
In one aspect, the generator 100 may comprise a DAC circuit 1308, 1412 and a power amplifier 1062, 422, 506. The DAC circuit 1308, 1412 is coupled to the power amplifier 212, 326, 426, 506 such that the DAC circuit 1308, 1412 provides the analog electrical signal waveform to a filter 1312, 1414 and the output of the filter 1312, 1414 is provided to the power amplifier 1062, 422, 506. The output of the power amplifier is provided to the surgical instrument 104, 108.
Further, in one aspect the generator 100 may be configured to provide the electrical signal waveform to at least two surgical instruments 104, 108 simultaneously. This may be accomplished through a single output port or channel of the generator 100. The generator 100 also may be configured to provide the electrical signal waveform, which may define two or more wave shapes, via a single output port or channel to the two surgical instruments 104, 108 simultaneously. The analog signal output of the generator 100 may define multiple wave shapes to one or more than one surgical instruments 104, 108. For example, in one aspect, the electrical signal waveform comprises multiple ultrasonic drive signals. In another aspect, the electrical signal waveform comprises multiple ultrasonic drive signals and one or more than one RF signals. Accordingly, an electrical signal waveform output of the generator 100 may comprise multiple ultrasonic drive signals, multiple RF signals, and/or a combination of multiple ultrasonic drive signals and a RF signals.
In one aspect, the generator 100 as described herein may allow for the creation of various types of direct digital synthesis lookup tables 1304, 1410 within an FPGA located in the generator 100. Some examples of the wave shapes that may be produced by the generator 100 include high crest factor signals (which may be used for surface coagulation), low crest factor signals (which may be used for deeper tissue penetration), and electrical signal waveforms that promote efficient touch-up coagulation. The generator 100 also may create multiple wave shape lookup tables 1304, 1410. The generator 100 can be configured to switch between different electrical signal waveforms for driving ultrasonic transducers 120 during a procedure (e.g., “on-the-fly” or in virtual real time based on user or sensor inputs) based on desired tissue effects or feedback signals associated with the state of the tissue located in the end effector 122, 125. Switching may be based on tissue impedance, tissue temperature, state of coagulation, state of dissection, and/or other factors.
In one aspect, the generator 100 as described herein also may provide, in addition to the traditional sine wave shape, wave shapes that maximizes the power into tissue per cycle (i.e. trapezoidal, square, or triangular wave shapes). It also may provide wave shapes that are synchronized in a manner that would maximize power delivery in the case of an electrical signal waveform comprises RF and ultrasonic signal components to drive ultrasonic and RF therapeutic energy simultaneously while maintaining ultrasonic frequency lock. Further, custom wave shapes specific to various types of surgical instruments 104, 108 and their tissue effects can be stored in a lookup table 1304, 1410 memory located in the generator 100 or the surgical instrument 104, 108, where the memory may be a volatile (RAM) or non-volatile (EEPROM) memory. The wave shape may be fetched from the lookup table 1304, 1410 memory upon connecting the surgical instrument 104, 108 to the generator 100.
With reference to
Further, in accordance with the method 2000, the digital processing circuit also instructs the DDS circuit 1300, 1400 to store 2008 a second digital electrical signal waveform in a second lookup table 1304, 1410 defined in the memory circuit, or other memory circuit. The second digital electrical signal waveform is represented by a second predetermined number of phase points that are stored in the second lookup table 1304, 1410. The second predetermined number of phase points define a second wave shape. The DDS circuit 1300, 1400 receives 2010 a clock signal. At each clock cycle, the DDS circuit 1300, 1400 retrieves 2012 a phase point from the second lookup table 1304, 1410. In one aspect, the second digital electrical signal waveform represents a second ultrasonic electrical signal waveform.
The digital signal processing circuit combines 2014 the retrieved phase point of the first digital electrical signal waveform and the retrieved phase point of the second digital electrical signal waveform to form a combined digital phase point. The combined digital phase point of the electrical signal waveform is converted 2016 by a DAC circuit 1308, 1412 to a combined analog signal. The analog signal 1310, 1420 output of the DAC circuit 1308, 1412 is filtered 2018 by a filter 1312, 1414 and is amplified 2020 by a power amplifier 212, 326, 426, 506 before the combined analog electrical signal waveform is provided to a surgical instrument 104, 108 connected to the generator 100. The first and second digital electrical signal waveforms may be combined in a way, for example using an appropriate algorithm, which is specifically designed to provide a proper input to a surgical instrument 104, 108. This may include limiting peaks of the combined digital electrical signal waveform so that the surgical instrument 104, 108 and/or components of the generator 100 are not damaged. Damage is one consequence of overdriving the components, however, another consequence is undesired wave shapes that can affect the ultrasonic transducer 120 or cause undesired output, such as unintended frequency components, on the RF poles. Accordingly, in one aspect, the output components are not damaged but are operating in a non-linear fashion and produce undesirable wave shapes, distortions, or harmonic components that could affect the operation of the ultrasonic transducer 120 or be delivered to tissue through the RF electrodes.
In one aspect, the combined analog electrical signal waveform is configured to drive a plurality of ultrasonic transducers 120, either simultaneously or sequentially. In another aspect, the combined analog electrical signal waveform is configured to drive a plurality of ultrasonic operational modes of an ultrasonic surgical instrument 104, 108. In one aspect, the ultrasonic surgical instrument 104, 108 comprises an ultrasonic transducer 120 and an ultrasonic blade 128, 149. The combined analog electrical signal waveform may be configured to drive the ultrasonic transducer 120 to produce a predetermined active length of the ultrasonic blade 128, 149. In one aspect, the combined analog electrical signal waveform may be configured to drive the ultrasonic transducer 120 to produce a predetermined tissue effect by the ultrasonic blade 128, 149.
In one aspect, the first and second digital electrical signal waveforms represent first and second digital ultrasonic electrical signal waveforms and the method 2000 further comprises combining a RF electrical signal waveform with the first and second ultrasonic electrical signal waveforms.
In one aspect, the digital processing circuit stores phase points of a digital electrical signal waveform in the lookup table 1304, 1410 defined by the memory circuit. The digital processing circuit stores phase points of multiple digital electrical signal waveforms in corresponding multiple lookup tables 1304, 1410 defined by the memory circuit or other memory circuits. Each of the digital electrical signal waveforms is represented by a predetermined number of phase points. Each of the predetermined number of phase points defines a different wave shape.
In one aspect, the digital processing circuit receives a feedback signal associated with tissue parameters and modifying the predetermined wave shape according to the feedback signal.
In one aspect, the digital electrical signal waveform represents a combination of two waveforms having different amplitudes. In one aspect, the digital electrical signal waveform represents a combination of two waveforms having different frequencies. In one aspect, the digital electrical signal waveform represents a combination of two waveforms having of different amplitudes. In one aspect, the wave shape is a trapezoid, a sine or cosine wave, a square wave, a triangle wave, or any combinations thereof. In one aspect, the combined digital signal waveform is configured to maintain a predetermined ultrasonic frequency. In one aspect, the combined digital signal waveform is configured to deliver maximum power output.
With reference to
A digitized ultrasonic electrical signal waveform, including a combined digital ultrasonic electrical signal waveform may be stored in a memory circuit defining a lookup table 1304, 1410 located either in the generator 100 or the surgical instrument 104, 106. The lookup table 1304, 1410 may be a direct digital synthesis table, located in the generator 100. The ultrasonic electrical signal waveform(s) and/or the combined ultrasonic electrical signal waveform(s) may consist of a plurality of phase points or samples stored in the memory circuit. In order for the generator 100 to output an analog ultrasonic electrical signal waveform made by combining two or more ultrasonic electrical signal waveforms, or other ultrasonic electrical signal waveform, the phase points are retrieved from the memory circuit by a digital processing circuit associated with the generator 100 or the surgical instrument 104, 108. As previously discussed, the phase points define the digital combined ultrasonic electrical signal waveform. The phase points are retrieved from the memory circuit upon connection of the surgical instrument 104, 108 to the generator 100. The phase points or digital samples may comprise at least 1,024 phase points. In other aspects the digital samples may comprise any number of phase points as shown in TABLE 1. Further, the analog version of the combined ultrasonic electrical signal waveform may be output to a surgical instrument 104, 108 via a single port of the generator 100 through which the surgical instrument 104, 108 is connected to the generator 100.
In one aspect, the generator 100, as described herein, may be a single port or multiple port system and may include an output transformer with multiple taps to provide the power in the form that is required for the treatment. In one aspect, the form may be higher voltage and lower current, in order to drive an ultrasonic transducer 120. In another aspect, the form may be lower voltage and higher current to drive vessel sealing electrodes. Or it may be a coagulation or type waveform for touch-up or spot coagulation.
In addition, the generator 100 may comprise a FPGA. The generator 100 may be configured to scan, via the FPGA, a lookup table 1304, 1410 comprising samples the digital electrical signal waveform, retrieve, via the FPGA, the stored phase points from the lookup table 1304, 1410, and provide the phase points to a DAC circuit 1308, 1412. The analog signal 1310, 1420 output of the DAC circuit 1308, 1412 is filtered by a filter 1312, 1414, and amplified by a power amplifier 1062, 422, 506. The amplified analog ultrasonic electrical signal waveform is then output from the generator 100 to the surgical instrument 104, 108.
The analog ultrasonic electrical signal waveform may be configured for a particular treatment modality of the surgical instrument 104, 108 connected to the generator 100. Accordingly, the ultrasonic electrical signal waveform may be a single or composite ultrasonic electrical signal waveform. In one aspect, the ultrasonic electrical signal waveform or the composite ultrasonic electrical signal waveform may be combined with a RF waveform, which may be provided to at least two surgical instruments 104, 108 simultaneously. The surgical instruments 104, 108 may comprise instruments that operate in the same modalities or different modalities of surgical treatment techniques. In one aspect, the surgical instruments 104, 108 include at least one ultrasonic surgical instrument 104 and at least one combination RF electrosurgical/ultrasonic surgical instrument. The electrical signal waveform also may be a combined RF and ultrasonic electrical signal waveform configured to maintain a predetermined ultrasonic frequency. In one aspect, the predetermined ultrasonic frequency is frequency locked when the surgical instrument 104, 108 is connected to the generator 100. In another aspect, the combined RF and ultrasonic electrical signal waveform is configured to cause the surgical instrument 104, 108 to deliver maximum power to the tissue engaged in the end effector 122, 125 of the surgical instrument 104, 108. The maximum power application may be based on the maximum power output of a treatment modality of a surgical instrument 104, 108, such as, for example, an RF modality and/or an ultrasonic modality. According to further aspects, the electrical signal waveform may comprise a high crest factor signal, a low crest factor signal, or a combination thereof and/or the electrical signal waveform may comprise a sine wave shape, a trapezoidal wave shape, a square wave shape, a triangular wave shape, or a combination thereof. The electrical signal waveform also may be configured to provide a desired tissue effect or outcome to tissue engaged by the end effector 122, 125 of the surgical instrument 104, 108 when the electrical signal waveform is received by the surgical instrument 104, 108. In one aspect, the desired tissue effect is at least one of cutting, coagulation, and/or sealing.
The generator 100 also may be configured to switch between a first electrical signal waveform and a second electrical signal waveform based on predetermined criteria, such as, for example, a desired tissue effect and/or feedback from a surgical instrument 104, 108, which may include measured values of a tissue parameter. The tissue parameter may include a tissue type, a tissue amount, a tissue state, or a combination thereof. Accordingly, the methods described above also may include delivering the first electrical signal waveform and the second electrical signal waveform based on a desired tissue effect, tissue parameter, and/or other parameters associated with a surgical instrument 104, 108 connected to the generator 100.
Additionally, the first and second digital electrical signal waveforms stored in the generator 100 may be received by the generator 100 from a surgical instrument 104, 108 connected to the generator 100. The generator 100 may receive the first and second digital electrical signal waveforms following or upon connecting the surgical instrument 104, 108 to the generator 100. The samples of the first and second digital electrical signal waveforms may be stored in an EEPROM of the surgical instrument 104, 108, which is operable coupled to the generator 100 upon connection of the surgical instrument 104, 108 to the generator 100.
In accordance with the methods 2200, 2300, 2400 the digital processing circuit instructs the DDS circuit 1300, 1400 to store phase points or samples that define a digital electrical signal waveform in a lookup table 1304, 1410 defined in the memory circuit. The digital electrical signal waveform is represented by a predetermined number of phase points that are stored in the lookup table 1304, 1410. The predetermined number of phase points define a predetermined wave shape. The DDS circuit 1300, 1400 receives a clock signal. At each clock cycle, the DDS circuit 1300, 1400 retrieves a phase point from the lookup table 1304, 1410 and provides the phase point (e.g., sample) to the DAC circuit 1308, 1412. The DAC circuit 1308, 1412 converts the phase point of the digital electrical signal waveform into an analog electrical signal output (e.g., a sample/hold output of the DAC circuit 1308, 1412). The analog sample/hold output of the DAC circuit 1308, 1412 is filtered by the filter 1312, 1414 and amplified by a power amplifier 212, 326, 426, 506 (
The one or more than one digital electrical signal waveforms may be generated from a one or more than one lookup tables 1304, 1410 as described in connection with
Additionally, digital phase points of the digital electrical signal waveform may be received by the generator 100 from a surgical instrument 104, 106, 108 connected to the generator 100. The generator 100 may receive the phase points following or upon connection of the surgical instrument 104, 106, 108 to the generator 100. The phase points of the digital electrical signal waveform may be stored in an EEPROM of the surgical instrument 104, 106, 108, which is operable coupled to the generator 100 upon connection of the surgical instrument 104, 106, 108 to the generator 100.
According to various aspects, the electrical signal waveform also may be provided to at least two surgical instruments 104, 106, 108 simultaneously. The surgical instruments 104, 106, 108 may comprise instruments that operate the same modalities or different modalities of surgical treatment techniques. In one aspect, the surgical instruments include at least one ultrasonic surgical instrument and at least one RF surgical instrument.
In various aspects, the electrical signal waveforms may represent electrical signals having different wave shapes. In one aspect, the electrical signal waveforms may represent ultrasonic signals suitable for driving ultrasonic transducers 120 of an ultrasonic surgical instrument 104, RF signals suitable for driving an electrode of an electrosurgical instrument 106 or a multifunction surgical instrument 108. A plurality of the electrical signal waveforms can be delivered separately, simultaneously, individually, or combined in one signal.
With reference now to
The first digital electrical signal waveform may include a RF drive signal and the second digital electrical signal waveform may include an ultrasonic drive signal. The first and/or the second digital electrical signal waveform may be generated via the DDS circuit 1300, 1400 of the generator 100. In one aspect, the method 1500 further comprises determining that the peak maximum amplitude of the combined digital electrical signal waveform is approaching as the combined digital electrical signal waveform is being delivered or transmitted to the surgical instrument 104, 106, 108. In another aspect, the method 2200 further comprises determining a peak amplitude of the combined digital electrical signal waveform and modifying the combined digital electrical signal waveform based on the peak amplitude of the combined waveform. In addition, the generator 100 may be configured to modify the combined digital electrical signal waveform by reducing the amplitude of the combined digital electrical signal waveform upon determining that the peak amplitude of the combined digital electrical signal waveform is approaching during transmission or delivery of the analog electrical signal waveform to the surgical instrument 104, 106, 108.
With reference now to
With reference now to
In various aspects, the first and second electrical signal waveforms may represent electrical signals having different wave shapes. In one aspect, the first digital electrical signal waveform may represent an RF signal suitable for driving an electrode of an RF electrosurgical instrument 106 or a multifunction surgical instrument 108 and the second electrical signal waveform may represent an ultrasonic signal for driving an ultrasonic transducer of an ultrasonic surgical instrument 104 or a multifunction surgical instrument 108. The first and second electrical signal waveforms can be delivered separately, simultaneously, individually, or combined in one signal.
While the examples herein are described mainly in the context of electrosurgical instruments, it should be understood that the teachings herein may be readily applied to a variety of other types of medical instruments. By way of example only, the teachings herein may be readily applied to tissue graspers, tissue retrieval pouch deploying instruments, surgical staplers, ultrasonic surgical instruments, etc. It should also be understood that the teachings herein may be readily applied to any of the instruments described in any of the references cited herein, such that the teachings herein may be readily combined with the teachings of any of the references cited herein in numerous ways. Other types of instruments into which the teachings herein may be incorporated will be apparent to those of ordinary skill in the art.
It should be appreciated that any patent, publication, or other disclosure material, in whole or in part, that is said to be incorporated by reference herein is incorporated herein only to the extent that the incorporated material does not conflict with existing definitions, statements, or other disclosure material set forth in this disclosure. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.
Aspects of the present disclosure have application in conventional endoscopic and open surgical instrumentation as well as application in robotic-assisted surgery. For instance, those of ordinary skill in the art will recognize that various teaching herein may be readily combined with various teachings of U.S. Pat. No. 6,783,524, titled ROBOTIC SURGICAL TOOL WITH ULTRASOUND CAUTERIZING AND CUTTING INSTRUMENT, published Aug. 31, 2004, the disclosure of which is incorporated by reference herein.
Aspects of the devices disclosed herein can be designed to be disposed of after a single use, or they can be designed to be used multiple times. Various aspects may, in either or both cases, be reconditioned for reuse after at least one use. Reconditioning may include any combination of the steps of disassembly of the device, followed by cleaning or replacement of particular pieces, and subsequent reassembly. In particular, aspects of the device may be disassembled, and any number of the particular pieces or parts of the device may be selectively replaced or removed in any combination. Upon cleaning and/or replacement of particular parts, aspects of the device may be reassembled for subsequent use either at a reconditioning facility, or by a surgical team immediately prior to a surgical procedure. Those skilled in the art will appreciate that reconditioning of a device may utilize a variety of techniques for disassembly, cleaning/replacement, and reassembly. Use of such techniques, and the resulting reconditioned device, are all within the scope of the present application.
By way of example only, aspects described herein may be processed before surgery. First, a new or used instrument may be obtained and if necessary cleaned. The instrument may then be sterilized. In one sterilization technique, the instrument is placed in a closed and sealed container, such as a plastic or TYVEK bag. The container and instrument may then be placed in a field of radiation that can penetrate the container, such as gamma radiation, x-rays, or high-energy electrons. The radiation may kill bacteria on the instrument and in the container. The sterilized instrument may then be stored in the sterile container. The sealed container may keep the instrument sterile until it is opened in a medical facility. A device may also be sterilized using any other technique known in the art, including but not limited to beta or gamma radiation, ethylene oxide, or steam.
Having shown and described various aspects of the present disclosure, further adaptations of the methods and systems described herein may be accomplished by appropriate modifications by one of ordinary skill in the art without departing from the scope of the present disclosure. Several of such potential modifications have been mentioned, and others will be apparent to those skilled in the art. For instance, the examples, aspects, geometrics, materials, dimensions, ratios, steps, and the like discussed above are illustrative and are not required. Accordingly, the scope of the present disclosure should be considered in terms of the following claims and is understood not to be limited to the details of structure and operation shown and described in the specification and drawings.
While various details have been set forth in the foregoing description, it will be appreciated that the various aspects of the techniques for operating a generator for digitally generating electrical signal waveforms and surgical instruments may be practiced without these specific details. One skilled in the art will recognize that the herein described components (e.g., operations), devices, objects, and the discussion accompanying them are used as examples for the sake of conceptual clarity and that various configuration modifications are contemplated. Consequently, as used herein, the specific exemplars set forth and the accompanying discussion are intended to be representative of their more general classes. In general, use of any specific exemplar is intended to be representative of its class, and the non-inclusion of specific components (e.g., operations), devices, and objects should not be taken limiting.
Further, while several forms have been illustrated and described, it is not the intention of the applicant to restrict or limit the scope of the appended claims to such detail. Numerous modifications, variations, changes, substitutions, combinations, and equivalents to those forms may be implemented and will occur to those skilled in the art without departing from the scope of the present disclosure. Moreover, the structure of each element associated with the described forms can be alternatively described as a means for providing the function performed by the element. Also, where materials are disclosed for certain components, other materials may be used. It is therefore to be understood that the foregoing description and the appended claims are intended to cover all such modifications, combinations, and variations as falling within the scope of the disclosed forms. The appended claims are intended to cover all such modifications, variations, changes, substitutions, modifications, and equivalents.
For conciseness and clarity of disclosure, selected aspects of the foregoing disclosure have been shown in block diagram form rather than in detail. Some portions of the detailed descriptions provided herein may be presented in terms of instructions that operate on data that is stored in a computer memory. Such descriptions and representations are used by those skilled in the art to describe and convey the substance of their work to others skilled in the art. In general, an algorithm refers to a self-consistent sequence of steps leading to a desired result, where a “step” refers to a manipulation of physical quantities which may, though need not necessarily, take the form of electrical or magnetic signals capable of being stored, transferred, combined, compared, and otherwise manipulated. It is common usage to refer to these signals as bits, values, elements, symbols, characters, terms, numbers, or the like. These and similar terms may be associated with the appropriate physical quantities and are merely convenient labels applied to these quantities.
Unless specifically stated otherwise as apparent from the foregoing disclosure, it is appreciated that, throughout the foregoing disclosure, discussions using terms such as “processing” or “computing” or “calculating” or “determining” or “displaying” or the like, refer to the action and processes of a computer system, or similar electronic computing device, that manipulates and transforms data represented as physical (electronic) quantities within the computer system's registers and memories into other data similarly represented as physical quantities within the computer system memories or registers or other such information storage, transmission or display devices.
In a general sense, those skilled in the art will recognize that the various aspects described herein which can be implemented, individually and/or collectively, by a wide range of hardware, software, firmware, or any combination thereof can be viewed as being composed of various types of “electrical circuitry.” Consequently, as used herein “electrical circuitry” includes, but is not limited to, electrical circuitry having at least one discrete electrical circuit, electrical circuitry having at least one integrated circuit, electrical circuitry having at least one application specific integrated circuit, electrical circuitry forming a general purpose computing device configured by a computer program (e.g., a general purpose computer configured by a computer program which at least partially carries out processes and/or devices described herein, or a microprocessor configured by a computer program which at least partially carries out processes and/or devices described herein), electrical circuitry forming a memory device (e.g., forms of random access memory), and/or electrical circuitry forming a communications device (e.g., a modem, communications switch, or optical-electrical equipment). Those having skill in the art will recognize that the subject matter described herein may be implemented in an analog or digital fashion or some combination thereof.
The foregoing detailed description has set forth various forms of the devices and/or processes via the use of block diagrams, flowcharts, and/or examples. Insofar as such block diagrams, flowcharts, and/or examples contain one or more functions and/or operations, it will be understood by those within the art that each function and/or operation within such block diagrams, flowcharts, or examples can be implemented, individually and/or collectively, by a wide range of hardware, software, firmware, or virtually any combination thereof. In one form, several portions of the subject matter described herein may be implemented via an application specific integrated circuits (ASIC), a field programmable gate array (FPGA), a digital signal processor (DSP), or other integrated formats. However, those skilled in the art will recognize that some aspects of the forms disclosed herein, in whole or in part, can be equivalently implemented in integrated circuits, as one or more computer programs running on one or more computers (e.g., as one or more programs running on one or more computer systems), as one or more programs running on one or more processors (e.g., as one or more programs running on one or more microprocessors), as firmware, or as virtually any combination thereof, and that designing the circuitry and/or writing the code for the software and or firmware would be well within the skill of one of skill in the art in light of this disclosure. In addition, those skilled in the art will appreciate that the mechanisms of the subject matter described herein are capable of being distributed as a program product in a variety of forms, and that an illustrative form of the subject matter described herein applies regardless of the particular type of signal bearing medium used to actually carry out the distribution. Examples of a signal bearing medium include, but are not limited to, the following: a recordable type medium such as a floppy disk, a hard disk drive, a Compact Disc (CD), a Digital Video Disk (DVD), a digital tape, a computer memory, etc.; and a transmission type medium such as a digital and/or an analog communication medium (e.g., a fiber optic cable, a waveguide, a wired communications link, a wireless communication link (e.g., transmitter, receiver, transmission logic, reception logic, etc.), etc.).
In some instances, one or more elements may be described using the expression “coupled” and “connected” along with their derivatives. It should be understood that these terms are not intended as synonyms for each other. For example, some aspects may be described using the term “connected” to indicate that two or more elements are in direct physical or electrical contact with each other. In another example, some aspects may be described using the term “coupled” to indicate that two or more elements are in direct physical or electrical contact. The term “coupled,” however, also may mean that two or more elements are not in direct contact with each other, but yet still co-operate or interact with each other. It is to be understood that depicted architectures of different components contained within, or connected with, different other components are merely examples, and that in fact many other architectures may be implemented which achieve the same functionality. In a conceptual sense, any arrangement of components to achieve the same functionality is effectively “associated” such that the desired functionality is achieved. Hence, any two components herein combined to achieve a particular functionality can be seen as “associated with” each other such that the desired functionality is achieved, irrespective of architectures or intermedial components. Likewise, any two components so associated also can be viewed as being “operably connected,” or “operably coupled,” to each other to achieve the desired functionality, and any two components capable of being so associated also can be viewed as being “operably couplable,” to each other to achieve the desired functionality. Specific examples of operably couplable include but are not limited to physically mateable and/or physically interacting components, and/or wirelessly interactable, and/or wirelessly interacting components, and/or logically interacting, and/or logically interactable components.
In other instances, one or more components may be referred to herein as “configured to,” “configurable to,” “operable/operative to,” “adapted/adaptable,” “able to,” “conformable/conformed to,” etc. Those skilled in the art will recognize that “configured to” can generally encompass active-state components and/or inactive-state components and/or standby-state components, unless context requires otherwise.
While particular aspects of the present disclosure have been shown and described, it will be apparent to those skilled in the art that, based upon the teachings herein, changes and modifications may be made without departing from the subject matter described herein and its broader aspects and, therefore, the appended claims are to encompass within their scope all such changes and modifications as are within the true scope of the subject matter described herein. It will be understood by those within the art that, in general, terms used herein, and especially in the appended claims (e.g., bodies of the appended claims) are generally intended as “open” terms (e.g., the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” the term “includes” should be interpreted as “includes but is not limited to,” etc.). It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases “at least one” and “one or more” to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles “a” or “an” limits any particular claim containing such introduced claim recitation to claims containing only one such recitation, even when the same claim includes the introductory phrases “one or more” or “at least one” and indefinite articles such as “a” or “an” (e.g., “a” and/or “an” should typically be interpreted to mean “at least one” or “one or more”); the same holds true for the use of definite articles used to introduce claim recitations.
In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should typically be interpreted to mean at least the recited number (e.g., the bare recitation of “two recitations,” without other modifiers, typically means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to “at least one of A, B, and C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, and C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). In those instances where a convention analogous to “at least one of A, B, or C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, or C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that typically a disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms unless context dictates otherwise. For example, the phrase “A or B” will be typically understood to include the possibilities of “A” or “B” or “A and B.”
With respect to the appended claims, those skilled in the art will appreciate that recited operations therein may generally be performed in any order. Also, although various operational flows are presented in a sequence(s), it should be understood that the various operations may be performed in other orders than those which are illustrated, or may be performed concurrently. Examples of such alternate orderings may include overlapping, interleaved, interrupted, reordered, incremental, preparatory, supplemental, simultaneous, reverse, or other variant orderings, unless context dictates otherwise. Furthermore, terms like “responsive to,” “related to,” or other past-tense adjectives are generally not intended to exclude such variants, unless context dictates otherwise.
It is worthy to note that any reference to “one aspect,” “an aspect,” “one form,” or “a form” means that a particular feature, structure, or characteristic described in connection with the aspect is included in at least one aspect. Thus, appearances of the phrases “in one aspect,” “in an aspect,” “in one form,” or “in an form” in various places throughout the specification are not necessarily all referring to the same aspect. Furthermore, the particular features, structures or characteristics may be combined in any suitable manner in one or more aspects.
With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations are not expressly set forth herein for sake of clarity.
In certain cases, use of a system or method may occur in a territory even if components are located outside the territory. For example, in a distributed computing context, use of a distributed computing system may occur in a territory even though parts of the system may be located outside of the territory (e.g., relay, server, processor, signal-bearing medium, transmitting computer, receiving computer, etc. located outside the territory).
A sale of a system or method may likewise occur in a territory even if components of the system or method are located and/or used outside the territory. Further, implementation of at least part of a system for performing a method in one territory does not preclude use of the system in another territory.
All of the above-mentioned U.S. patents, U.S. patent application publications, U.S. patent applications, foreign patents, foreign patent applications, non-patent publications referred to in this specification and/or listed in any Application Data Sheet, or any other disclosure material are incorporated herein by reference, to the extent not inconsistent herewith. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.
In summary, numerous benefits have been described which result from employing the concepts described herein. The foregoing description of the one or more forms has been presented for purposes of illustration and description. It is not intended to be exhaustive or limiting to the precise form disclosed. Modifications or variations are possible in light of the above teachings. The one or more forms were chosen and described in order to illustrate principles and practical application to thereby enable one of ordinary skill in the art to utilize the various forms and with various modifications as are suited to the particular use contemplated. It is intended that the claims submitted herewith define the overall scope.
Various aspects of the subject matter described herein are set out in the following numbered clauses:
1. An apparatus comprising a generator configured to provide an electrical signal waveform to at least one surgical instrument; a table comprising information associated with a plurality of wave shapes; and wherein the electrical signal waveform corresponds to at least one wave shape of the plurality of wave shapes of the table.
2. The apparatus of clause 1, wherein the table is stored within the generator.
3. The apparatus of clauses 1 or 2, wherein the table is a direct digital synthesis table.
4. The apparatus of clause 3, wherein the direct digital synthesis table is addressed according to a frequency of the electrical signal waveform.
5. The apparatus of any of clauses 1-4, wherein the information associated with the plurality of wave shapes is stored as digital information.
6. The apparatus of any of clauses 1-5, wherein the generator comprises a DAC circuit and a power amplifier, and wherein the DAC circuit is coupled to the power amplifier and the DAC circuit provides digital input values to the power amplifier associated with a wave shape of the plurality of wave shapes for the electrical signal waveform.
7. The apparatus of any of clauses 1-6, wherein the generator is configured to provide the electrical signal waveform to at least two surgical instruments simultaneously.
8. The apparatus of clause 7, wherein the electrical signal waveform provided to the at least two surgical instruments comprises at least two wave shapes.
9. The apparatus of clause 8, wherein the generator is configured to provide the electrical signal waveform that comprises the at least two wave shapes via a single output channel.
10. The apparatus of any of clauses 1-9, wherein the electrical signal waveform comprises an ultrasonic signal.
11. The apparatus of clause 10, wherein the electrical signal waveform is configured to control at least one of an output current, an output voltage, or an output power of an ultrasonic transducer.
12. The apparatus of clause 10 or 11, wherein the electrical signal waveform is configured to drive at least two vibration modes of an ultrasonic transducer of the at least one surgical instrument.
13. The apparatus of any of clauses 1-12, wherein the generator is configured to provide the electrical signal waveform to at least two surgical instruments simultaneously, wherein the electrical signal waveform comprises an ultrasonic signal and an RF signal.
14. A method of operating a generator, comprising: generating an electrical signal waveform; providing the generated electrical signal waveform to at least one surgical instrument; and wherein generating the electrical signal waveform comprises reading electrical signal waveform information from a table comprising information associated with a plurality of wave shapes; and wherein the generated electrical signal waveform corresponds to at least one wave shape of the plurality of wave shapes of the table.
15. The method of clause 14, wherein the generated electrical signal waveform corresponds to at least two wave shapes of the plurality of wave shapes of the table.
16. The method of clause 14 or 15, wherein the electrical signal waveform comprises an ultrasonic signal.
17. The method of any of clauses 14-16, wherein providing the generated electrical signal waveform to the at least one surgical instrument comprises providing the electrical signal waveform to at least two surgical instruments simultaneously.
18. The method of clause 17, wherein the at least two surgical instruments comprise at least one ultrasonic surgical instrument and at least one RF surgical instrument.
19. The method of clauses 14-18, wherein providing the generated electrical signal waveform comprises providing the generated waveform via a single output channel.
20. The method of clauses 14-19, wherein the table is a direct digital synthesis table that is addressed according to a frequency of the electrical signal waveform.
21. An apparatus for operating a surgical instrument, comprising: at least one surgical instrument configured to receive an electrical signal waveform from a generator; wherein the electrical signal waveform corresponds to at least one wave shape of a plurality of wave shapes stored in a table of the generator.
22. The apparatus of clause 21, wherein the at least one surgical instrument comprises at least two surgical instruments that receive the electrical signal waveform simultaneously.
23. The apparatus of clause 22, wherein the electrical signal waveform provided to the at least two surgical instruments comprises at least two wave shapes.
24. The apparatus of clause 22 or 23, wherein each of the at least two surgical instruments receive the electrical signal waveform from a single output channel of the generator.
25. The apparatus of any one of clauses 22-24, wherein one of the at least two surgical instruments comprises an ultrasonic surgical component and wherein another of the at least two surgical instruments comprises an RF surgical component.
26. The apparatus of any one of clauses 21-25, wherein the electrical signal waveform comprises a ultrasonic signal.
27. The apparatus of any of clauses 21-26, wherein the electrical signal waveform is configured to control at least one of an output current, an output voltage, or an output power of an ultrasonic transducer of the at least one surgical instrument.
28. The apparatus of any one of clauses 21-27, wherein the electrical signal waveform is configured to drive at least two vibration modes of an ultrasonic transducer of the at least one surgical instrument.
29. The apparatus of any one of clauses 21-28, wherein the generator is configured to provide the electrical signal waveform to at least two surgical instruments simultaneously.
30. A method of generating electrical signal waveforms by a generator, the generator comprising a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the memory circuit defining a lookup table, the method comprising: storing, by the digital processing circuit, phase points of a digital electrical signal waveform in the lookup table defined by the memory circuit, wherein the digital electrical signal waveform is represented by a predetermined number of phase points, wherein the predetermined number phase points define a predetermined wave shape; receiving a clock signal by the digital synthesis circuit, and at each clock cycle: retrieving, by the digital processing circuit, a phase point from the lookup table; and converting, by the DAC circuit, the retrieved phase point to an analog signal.
31. The method of clause 30, comprising amplifying, by an amplifier, the analog signal from an output of the DAC circuit.
32. The method of any one of clause 30 or 31, wherein storing, by the digital processing circuit, phase points of a digital electrical signal waveform in the lookup table defined by the memory circuit, comprises: storing, by the digital processing circuit, phase points of multiple digital electrical signal waveforms in corresponding multiple lookup tables defined by the memory circuit or other memory circuits, wherein each of the digital electrical signal waveforms is represented by a predetermined number of phase points, and wherein each of the predetermined number of phase points defines a different wave shape.
33. The method of any one of clauses 30-32, comprising: receiving, by the digital processing circuit, a feedback signal associated with tissue parameters; and modifying the predetermined wave shape according to the feedback signal.
34. The method of any one of clauses 30-33, wherein the digital electrical signal waveform represents a RF signal waveform, an ultrasonic signal waveform, or a combination thereof.
35. The method of any one of clauses 30-34, wherein the digital electrical signal waveform represents a combination of two waveforms having different amplitudes.
36. The method of any one of clauses 30-35, wherein the digital electrical signal waveform represents a combination of two waveforms having different frequencies.
37. The method of clause 36, wherein the digital electrical signal waveform represents a combination of two waveforms having of different amplitudes.
38. The method of any one of clauses 30-37, wherein the predetermined wave shape is a trapezoid, a sine or cosine wave, a square wave, a triangle wave, or any combinations thereof.
39. The method of any one of clauses 30-38, wherein the digital electrical signal waveform is a combined RF and ultrasonic signal waveform configured to maintain a predetermined ultrasonic frequency.
40. The method of any one of clauses 30-39, wherein the first is a combined RF and ultrasonic waveform configured to deliver maximum power output.
41. A method of generating electrical signal waveforms by a generator, the generator comprising a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the memory circuit defining first and second lookup tables, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; receiving, by the digital synthesis circuit, a clock signal, and at each clock cycle: retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; and determining, by the digital processing circuit, whether to switch between the phase points of the first and second electrical signal waveforms or to synchronize the phase points of the first and second electrical signal waveforms.
42. The method of clause 41, comprising receiving, by the digital processing circuit, a feedback signal associated with tissue parameters.
43. The method of clause 42, comprising: switching between the phase point of the first digital electrical signal waveform and the phase point of the second digital electrical signal waveform; and converting, by the DAC circuit, the retrieved phase point.
44. The method of clause 42, comprising: synchronizing the phase points of the first and second digital electrical signal waveforms to maximize power delivery per cycle; and converting, by the DAC circuit, the synchronized phase points.
45. The method of any one of clauses 41-44, wherein the first digital electrical signal waveform represents a RF waveform and the second digital electrical signal waveform represents an ultrasonic signal waveform.
46. A generator for generating electrical signal waveforms, the generator comprising: a digital processing circuit; a memory circuit in communication with the digital processing circuit, the memory circuit defining a lookup table; a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, the digital synthesis circuit receiving a clock signal; and a digital-to-analog converter (DAC) circuit; the digital processing circuit configured to store phase points of a digital electrical signal waveform in the lookup table defined by the memory circuit, wherein the digital electrical signal waveform is represented by a predetermined number of phase points, wherein the predetermined number phase points define a predetermined wave shape; and retrieve a phase point from the lookup table at each clock cycle; and the DAC circuit configured to convert the retrieved phase point to an analog signal.
47. The generator of clause 46, comprising an amplifier coupled to the DAC circuit.
48. The generator of clause 46 or 47, wherein the digital synthesis circuit is a direct digital synthesis (DDS) circuit.
49. The generator of any one of clauses 46-48, comprising a filter coupled to the output of the DAC circuit.
50. A method of generating electrical signal waveforms by a generator, the generator comprising a digital processing circuit, a memory circuit in communication with the digital processing circuit, the memory circuit defining first and second lookup tables, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; and receiving a clock signal by the digital synthesis circuit, and at each clock cycle: retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; combining, by the digital processing circuit, the phase point from the first lookup table with the phase point from the second lookup table to generate a combined phase point; and converting, by the DAC circuit, the combined phase point into an analog signal; wherein the analog signal is configured to drive a first and second ultrasonic transducer.
51. The method of clause 50, wherein the first and second digital electrical signal waveforms represent first and second digital ultrasonic electrical signal waveforms.
52. The method of clause 50 or 51, comprising combining a radio frequency (RF) electrical signal waveform with the first and second ultrasonic electrical signal waveforms.
53. The method of any one of clauses 50-52, wherein storing, by the digital processing circuit, phase points of a digital electrical signal waveform in the lookup table defined by the memory circuit, comprises: storing, by the digital processing circuit, phase points of multiple digital electrical signal waveforms in corresponding multiple lookup tables defined by the memory circuit or other memory circuits, wherein each of the digital electrical signal waveforms is represented by a predetermined number of phase points, and wherein each of the predetermined number of phase points defines a different wave shape.
54. The method of any one of clauses 50-53, comprising: receiving, by the digital processing circuit, a feedback signal associated with tissue parameters; and modifying the first or second predetermined wave shape according to the feedback signal.
55. The method of any one of clauses 50-54, wherein the first or second digital electrical signal waveform represents a combination of multiple waveforms having different amplitudes.
56. The method of any one of clauses 50-55, wherein the first or second digital electrical signal waveform represents a combination of multiple waveforms having different frequencies.
57. The method of clause 56, wherein the first or second digital electrical signal waveform represents a combination of multiple waveforms having of different amplitudes.
58. The method of any one of clauses 50-57, wherein the first or second predetermined wave shape is a trapezoid, a sine or cosine wave, a square wave, a triangle wave, or any combinations thereof.
59. The method of any one of clauses 50-58, wherein the combined phase point is configured to maintain a predetermined ultrasonic frequency.
60. The method of any one of clauses 50-59, wherein the combined phase point is configured to deliver maximum power output.
61. A method of generating electrical signal waveforms by a generator, the generator comprising a digital processing circuit, a memory circuit in communication with the digital processing circuit, the memory circuit defining first and second lookup tables, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; and receiving a clock signal by the digital synthesis circuit, and at each clock cycle: retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; combining, by the digital processing circuit, the phase point from the first lookup table with the phase point from the second lookup table to generate a combined phase point; and converting, by the DAC circuit, the combined phase point into an analog signal; wherein the analog signal is configured to drive a plurality of ultrasonic operational modes of an ultrasonic device.
62. The method of clause 61, wherein the analog signal is configured to provide a predetermined tissue effect.
63. The method of clauses 61 or 62, wherein the generator comprises a single output port and the method further comprises delivering the analog signal via the single output port.
64. A generator for generating electrical signal waveforms, the generator comprising: a digital processing circuit; a memory circuit in communication with the digital processing circuit, the memory circuit defining a lookup table; a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, the digital synthesis circuit receiving a clock signal; and a digital-to-analog converter (DAC) circuit; the digital processing circuit configured to: store phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; and store phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; at each clock cycle the digital synthesis circuit is configured to: retrieve a phase point from the first lookup table; retrieve a phase point from the second lookup table; the digital processing circuit configured to: combine the phase point from the first lookup table with the phase point from the second lookup table to generate a combined phase point; and the DAC circuit is configured to convert the combined phase point into an analog signal; wherein the analog signal is configured to drive a first and second ultrasonic transducer.
65. The generator of clause 64, comprising a non-volatile memory.
66. The generator of clauses 64 or 65, comprising a field programmable gate array (FPGA).
67. The generator of any one of clauses 64-66, comprising an amplifier coupled to the DAC circuit.
68. The generator of any one of clauses 64-67, wherein the digital synthesis circuit is a direct digital synthesis (DDS) circuit.
69. The generator of any one of clauses 64-68, comprising a filter coupled to an output of the DAC circuit.
70. A method of generating electrical signal waveforms by a generator, the generator comprising a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the memory circuit defining first and second lookup tables, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape; receiving, by the digital synthesis circuit, a clock signal, and at each clock cycle; retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; combining, by the digital processing circuit, the first and second digital electrical signal waveforms to form a combined digital electrical signal waveform; and modifying, by the digital processing circuit, the combined digital electrical signal waveform to form a modified digital electrical signal waveform, wherein a peak amplitude of the modified digital electrical signal waveform does not exceed a predetermined amplitude value.
71. The method of clause 70, comprising defining, by the digital processing circuit, the first or second digital electrical signal waveform as a radio frequency (RF) drive signal.
72. The method of clause 70 or 71, comprising defining, by the digital processing circuit, the first or second digital electrical signal waveform as an ultrasonic drive signal.
73. The method of any one of clauses 70-72, comprising determining, by the digital processing circuit, the peak amplitude of the combined digital electrical signal waveform while the combined digital electrical signal waveform is being delivered.
74. The method of clause 73, wherein modifying the combined digital electrical signal waveform comprises reducing an amplitude of the combined digital electrical signal waveform upon determining that the peak amplitude of the combined digital electrical signal waveform is approaching while the combined digital electrical signal waveform is being delivered.
75. The method of any one of clauses 70-74, wherein the generator comprises a direct digital synthesis (DDS) circuit and wherein generating the first or second digital electrical signal waveform comprises generating the first or second digital electrical signal waveform via the DDS circuit.
76. The method of any one of clauses 70-75, comprising determining a peak amplitude of the combined waveform and wherein modifying the combined waveform comprises modifying the combined waveform based on the peak amplitude of the combined waveform.
77. The method of any one of clauses 70-76, comprising converting, by the DAC circuit, the digital electrical signal waveform to an analog signal and outputting the analog signal.
78. The method of clause 77, wherein the generator comprises a transformer with a plurality of taps, the method comprises outputting the analog signal via a single port of the generator.
79. A method of generating electrical signal waveforms by a generator, the generator comprising a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the memory circuit defining first and second lookup tables, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape, wherein the second digital electrical signal waveform is a function of the first digital electrical signal waveform; receiving, by the digital synthesis circuit, a clock signal, and at each clock cycle; retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; combining, by the digital processing circuit, the first and second digital electrical signal waveforms to form a combined digital electrical signal waveform; and modifying, by the digital processing circuit, the combined digital electrical signal waveform to form a modified digital electrical signal waveform, wherein a peak amplitude of the modified digital electrical signal waveform does not exceed a predetermined amplitude value.
80. The method of clause 79, comprising extracting, by the digital processing circuit, the first or second digital electrical signal waveform from the combined digital electrical signal waveform.
81. The method of clause 80, wherein the first or second digital electrical signal waveform comprises a wave function, the method comprising extracting the wave function from the combined digital electrical signal waveform.
82. The method of any one of clauses 80-81, comprising outputting the combined digital electrical signal waveform via a single port of the generator.
83. The method of any one of clauses 80-82, comprising defining, by the digital processing circuit, the first or second digital electrical signal waveform as an ultrasonic drive signal.
84. The method of any one of clauses 80-83, comprising defining, by the digital processing circuit, the first or second digital electrical signal waveform as a radio frequency (RF) drive signal.
85. A method of generating electrical signal waveforms by a generator, the generator comprising a digital processing circuit, a memory circuit in communication with the digital processing circuit, a digital synthesis circuit in communication with the digital processing circuit and the memory circuit, and a digital-to-analog converter (DAC) circuit, the memory circuit defining first and second lookup tables, the method comprising: storing, by the digital processing circuit, phase points of a first digital electrical signal waveform in a first lookup table defined by the memory circuit, wherein the first digital electrical signal waveform is represented by a first predetermined number of phase points, wherein the first predetermined number of phase points define a first predetermined wave shape; storing, by the digital processing circuit, phase points of a second digital electrical signal waveform in a second lookup table defined by the memory circuit, wherein the second digital electrical signal waveform is represented by a second predetermined number of phase points, wherein the second predetermined number of phase points define a second predetermined wave shape, wherein the second digital electrical signal waveform is a function of the first digital electrical signal waveform; receiving, by the digital synthesis circuit, a clock signal, and at each clock cycle; retrieving, by the digital synthesis circuit, a phase point from the first lookup table; retrieving, by the digital synthesis circuit, a phase point from the second lookup table; modifying, by the digital processing circuit, a frequency of the first digital electrical signal waveform to form a frequency modified first digital electrical signal waveform; and combining, by the digital processing circuit, the frequency modified first digital electrical signal waveform and the second digital electrical signal waveform to form a combined digital electrical signal waveform.
86. The method of clause 85, comprising defining, by the digital processing circuit, the first or second digital electrical signal waveform as a radio frequency (RF) drive signal.
87. The method of clauses 85-86, comprising defining, by the digital processing circuit, the first or second digital electrical signal waveform as an ultrasonic drive signal.
88. The method of any one of clauses 85-87, comprising outputting the combined digital electrical signal waveform via a single port of the generator.
89. The method of any one of clauses 85-88, wherein the generator comprises a direct digital synthesis (DDS) circuit, wherein generating the first digital electrical signal waveform comprises generating the first or second digital electrical signal waveform via the DDS circuit.
90. A method of generating electrical signal waveforms by a generator, the generator comprising a processor and a memory in communication with the processor, the memory defining a first and second table, the method comprising: retrieving, by the processor, information from the first table defined the memory, wherein the information is associated with a first wave shape of a first electrical signal waveform for performing a surgical procedure; retrieving, by the processor, information from the second table defined in the memory, wherein the information is associated with a second wave shape of a second electrical signal waveform for performing a surgical procedure; combining, by the processor, the first and second wave shapes to create a combined wave shape of an electrical signal waveform for performing a surgical procedure; and delivering the combined wave shape electrical signal waveform for performing a surgical procedure to a surgical instrument.
91. The method of clause 90, wherein the first table is defined by the first memory and the second table is defined by a second memory.
92. The method of clause 90 or 91, wherein the first wave shape is associated with a radio frequency (RF) electrical signal waveform and the second wave shape is associated with an ultrasonic electrical signal waveform.
93. The method of any one of clauses 90-92, wherein the first wave shape is associated with a first ultrasonic electrical signal waveform and the second wave shape is associated with a second ultrasonic electrical signal waveform.
94. The method of any one of clauses 90-93, comprising creating the first and second table by a direct digital synthesis circuit coupled to the processor.
95. The method of clause 94, comprising: addressing, by the processor, the first table according to a frequency of the first electrical signal waveform; and addressing, by the processor, the second table according to a frequency of the second electrical signal waveform.
96. The method of clause 94, comprising: storing, by the processor, the information associated with the first wave shape in the memory; and storing, by the processor, the information associated with the second wave shape
97. The method of any one of clauses 90-96, comprising: receiving, by the processor, a feedback signal associated with tissue parameters; and modifying the first and second wave shapes according to the feedback signal.
98. A method of generating electrical signal waveforms by a generator, the generator comprising a processor and a memory in communication with the processor, the memory defining a first and second table, the method comprising: retrieving, by the processor, information from the first table defined the memory, wherein the information is associated with a first wave shape of a first electrical signal waveform for performing a surgical procedure; retrieving, by the processor, information from the second table defined in the memory, wherein the information is associated with a second wave shape of a second electrical signal waveform for performing a surgical procedure; and delivering the first and second electrical signal waveforms for performing a surgical procedure to a surgical instrument.
99. The method of clause 98, comprising switching between the first and second electrical signal waveforms.
100. The method of clause 98 or 99, comprising: synchronizing the first and second electrical signal waveforms; and maximizing power delivered to the surgical instrument.
101. The method of any one of clauses 98-100, wherein the first digital electrical signal waveform represents a RF waveform and the second digital electrical signal waveform represents an ultrasonic signal waveform.
102. The method of any one of clauses 98-101, wherein the first wave shape is associated with a first ultrasonic electrical signal waveform and the second wave shape is associated with a second ultrasonic electrical signal waveform.
103. A method of generating electrical signal waveforms by a generator, the generator comprising a processor and a memory in communication with the processor, the memory defining a first and second table, the method comprising: retrieving, by the processor, information from the first table defined the memory, wherein the information is associated with a first wave shape of a first electrical signal waveform for performing a surgical procedure; retrieving, by the processor, information from the second table defined in the memory, wherein the information is associated with a second wave shape of a second electrical signal waveform for performing a surgical procedure; and combining, by the processor, the first and second wave shapes to create a combined wave shape of an electrical signal waveform for performing a surgical procedure; delivering the combined wave shape electrical signal waveform for performing a surgical procedure to a surgical instrument; and modifying, by the processor, the combined wave shape of the electrical signal waveform to form a modified electrical signal waveform, wherein a peak amplitude of the modified electrical signal waveform does not exceed a predetermined amplitude.
104. The method of clause 103, wherein the first wave shape is associated with a first radio frequency (RF) electrical signal waveform and the second wave shape is associated with a second RF electrical signal waveform.
105. The method of clause 103 or 104, wherein the first wave shape is associated with a first ultrasonic electrical signal waveform and the second wave shape is associated with a second ultrasonic electrical signal waveform.
106. The method of any one of clauses 103-105, wherein the first wave shape is associated with a RF electrical signal waveform and the second wave shape is associated with an ultrasonic electrical signal waveform.
107. The method of any one of clauses 103-106, comprising determining, by the processor, the peak amplitude of the combined electrical signal waveform while delivering the combined electrical signal waveform to the surgical instrument.
108. The method of any one of clauses 103-107, comprising reducing an amplitude of the combined electrical signal waveform when the peak amplitude of the combined electrical signal waveform is approaching.
109. The method of any one of clauses 103-108, comprising determining a peak amplitude of the combined electrical signal waveform and modifying the combined electrical signal waveform comprises based on the determined peak amplitude of the combined electrical signal waveform.
This application claims the benefit of U.S. Provisional Application Ser. No. 62/235,260, titled GENERATOR FOR PROVIDING COMBINED RADIO FREQUENCY AND ULTRASONIC ENERGIES, filed Sep. 30, 2015, U.S. Provisional Application Ser. No. 62/235,368, titled CIRCUIT TOPOLOGIES FOR GENERATOR, filed Sep. 30, 2015, and U.S. Provisional Application Ser. No. 62/235,466, titled SURGICAL INSTRUMENT WITH USER ADAPTABLE ALGORITHMS, filed Sep. 30, 2015, the contents of each of which are incorporated herein by reference in their entirety.
Number | Name | Date | Kind |
---|---|---|---|
969528 | Disbrow | Sep 1910 | A |
1570025 | Young | Jan 1926 | A |
1813902 | Bovie | Jul 1931 | A |
2188497 | Calva | Jan 1940 | A |
2366274 | Luth et al. | Jan 1945 | A |
2425245 | Johnson | Aug 1947 | A |
2442966 | Wallace | Jun 1948 | A |
2458152 | Eakins | Jan 1949 | A |
2510693 | Green | Jun 1950 | A |
2597564 | Bugg | May 1952 | A |
2704333 | Calosi et al. | Mar 1955 | A |
2736960 | Armstrong | Mar 1956 | A |
2748967 | Roach | Jun 1956 | A |
2845072 | Shafer | Jul 1958 | A |
2849788 | Creek | Sep 1958 | A |
2867039 | Zach | Jan 1959 | A |
2874470 | Richards | Feb 1959 | A |
2990616 | Balamuth et al. | Jul 1961 | A |
RE25033 | Balamuth et al. | Aug 1961 | E |
3015961 | Roney | Jan 1962 | A |
3033407 | Alfons | May 1962 | A |
3053124 | Balamuth et al. | Sep 1962 | A |
3082805 | Royce | Mar 1963 | A |
3166971 | Stoecker | Jan 1965 | A |
3322403 | Murphy | May 1967 | A |
3432691 | Shoh | Mar 1969 | A |
3433226 | Boyd | Mar 1969 | A |
3489930 | Shoh | Jan 1970 | A |
3513848 | Winston et al. | May 1970 | A |
3514856 | Camp et al. | Jun 1970 | A |
3525912 | Wallin | Aug 1970 | A |
3526219 | Balamuth | Sep 1970 | A |
3554198 | Tatoian et al. | Jan 1971 | A |
3580841 | Cadotte et al. | May 1971 | A |
3606682 | Camp et al. | Sep 1971 | A |
3614484 | Shoh | Oct 1971 | A |
3616375 | Inoue | Oct 1971 | A |
3629726 | Popescu | Dec 1971 | A |
3636943 | Balamuth | Jan 1972 | A |
3668486 | Silver | Jun 1972 | A |
3702948 | Balamuth | Nov 1972 | A |
3703651 | Blowers | Nov 1972 | A |
3776238 | Peyman et al. | Dec 1973 | A |
3777760 | Essner | Dec 1973 | A |
3805787 | Banko | Apr 1974 | A |
3809977 | Balamuth et al. | May 1974 | A |
3830098 | Antonevich | Aug 1974 | A |
3854737 | Gilliam, Sr. | Dec 1974 | A |
3862630 | Balamuth | Jan 1975 | A |
3875945 | Friedman | Apr 1975 | A |
3885438 | Harris, Sr. et al. | May 1975 | A |
3900823 | Sokal et al. | Aug 1975 | A |
3918442 | Nikolaev et al. | Nov 1975 | A |
3924335 | Balamuth et al. | Dec 1975 | A |
3946738 | Newton et al. | Mar 1976 | A |
3955859 | Stella et al. | May 1976 | A |
3956826 | Perdreaux, Jr. | May 1976 | A |
4005714 | Hiltebrandt | Feb 1977 | A |
4012647 | Balamuth et al. | Mar 1977 | A |
4034762 | Cosens et al. | Jul 1977 | A |
4058126 | Leveen | Nov 1977 | A |
4074719 | Semm | Feb 1978 | A |
4156187 | Murry et al. | May 1979 | A |
4167944 | Banko | Sep 1979 | A |
4188927 | Harris | Feb 1980 | A |
4200106 | Douvas et al. | Apr 1980 | A |
4203430 | Takahashi | May 1980 | A |
4203444 | Bonnell et al. | May 1980 | A |
4220154 | Semm | Sep 1980 | A |
4237441 | van Konynenburg et al. | Dec 1980 | A |
4281785 | Brooks | Aug 1981 | A |
4300083 | Heiges | Nov 1981 | A |
4302728 | Nakamura | Nov 1981 | A |
4304987 | van Konynenburg | Dec 1981 | A |
4306570 | Matthews | Dec 1981 | A |
4314559 | Allen | Feb 1982 | A |
4353371 | Cosman | Oct 1982 | A |
4409981 | Lundberg | Oct 1983 | A |
4445063 | Smith | Apr 1984 | A |
4463759 | Garito et al. | Aug 1984 | A |
4491132 | Aikins | Jan 1985 | A |
4492231 | Auth | Jan 1985 | A |
4494759 | Kieffer | Jan 1985 | A |
4504264 | Kelman | Mar 1985 | A |
4512344 | Barber | Apr 1985 | A |
4526571 | Wuchinich | Jul 1985 | A |
4535773 | Yoon | Aug 1985 | A |
4541638 | Ogawa et al. | Sep 1985 | A |
4545374 | Jacobson | Oct 1985 | A |
4545926 | Fouts, Jr. et al. | Oct 1985 | A |
4549147 | Kondo | Oct 1985 | A |
4550870 | Krumme et al. | Nov 1985 | A |
4553544 | Nomoto et al. | Nov 1985 | A |
4562838 | Walker | Jan 1986 | A |
4574615 | Bower et al. | Mar 1986 | A |
4582236 | Hirose | Apr 1986 | A |
4593691 | Lindstrom et al. | Jun 1986 | A |
4617927 | Manes | Oct 1986 | A |
4633119 | Thompson | Dec 1986 | A |
4634420 | Spinosa et al. | Jan 1987 | A |
4640279 | Beard | Feb 1987 | A |
4641053 | Takeda | Feb 1987 | A |
4646738 | Trott | Mar 1987 | A |
4646756 | Watmough et al. | Mar 1987 | A |
4649919 | Thimsen et al. | Mar 1987 | A |
4662068 | Polonsky | May 1987 | A |
4674502 | Imonti | Jun 1987 | A |
4694835 | Strand | Sep 1987 | A |
4708127 | Abdelghani | Nov 1987 | A |
4712722 | Hood et al. | Dec 1987 | A |
4735603 | Goodson et al. | Apr 1988 | A |
4761871 | O'Connor et al. | Aug 1988 | A |
4808154 | Freeman | Feb 1989 | A |
4819635 | Shapiro | Apr 1989 | A |
4827911 | Broadwin et al. | May 1989 | A |
4830462 | Karny et al. | May 1989 | A |
4832683 | Idemoto et al. | May 1989 | A |
4836186 | Scholz | Jun 1989 | A |
4838853 | Parisi | Jun 1989 | A |
4844064 | Thimsen et al. | Jul 1989 | A |
4849133 | Yoshida et al. | Jul 1989 | A |
4850354 | McGurk-Burleson et al. | Jul 1989 | A |
4852578 | Companion et al. | Aug 1989 | A |
4860745 | Farin et al. | Aug 1989 | A |
4862890 | Stasz et al. | Sep 1989 | A |
4865159 | Jamison | Sep 1989 | A |
4867157 | McGurk-Burleson et al. | Sep 1989 | A |
4878493 | Pasternak et al. | Nov 1989 | A |
4880015 | Nierman | Nov 1989 | A |
4881550 | Kothe | Nov 1989 | A |
4896009 | Pawlowski | Jan 1990 | A |
4903696 | Stasz et al. | Feb 1990 | A |
4910389 | Sherman et al. | Mar 1990 | A |
4915643 | Samejima et al. | Apr 1990 | A |
4920978 | Colvin | May 1990 | A |
4922902 | Wuchinich et al. | May 1990 | A |
4936842 | D'Amelio et al. | Jun 1990 | A |
4954960 | Lo et al. | Sep 1990 | A |
4965532 | Sakurai | Oct 1990 | A |
4979952 | Kubota et al. | Dec 1990 | A |
4981756 | Rhandhawa | Jan 1991 | A |
5001649 | Lo et al. | Mar 1991 | A |
5009661 | Michelson | Apr 1991 | A |
5013956 | Kurozumi et al. | May 1991 | A |
5015227 | Broadwin et al. | May 1991 | A |
5020514 | Heckele | Jun 1991 | A |
5026370 | Lottick | Jun 1991 | A |
5026387 | Thomas | Jun 1991 | A |
5035695 | Weber, Jr. et al. | Jul 1991 | A |
5042707 | Taheri | Aug 1991 | A |
5061269 | Muller | Oct 1991 | A |
5075839 | Fisher et al. | Dec 1991 | A |
5084052 | Jacobs | Jan 1992 | A |
5099840 | Goble et al. | Mar 1992 | A |
5104025 | Main et al. | Apr 1992 | A |
5105117 | Yamaguchi | Apr 1992 | A |
5106538 | Barma et al. | Apr 1992 | A |
5108383 | White | Apr 1992 | A |
5109819 | Custer et al. | May 1992 | A |
5112300 | Ureche | May 1992 | A |
5113139 | Furukawa | May 1992 | A |
5123903 | Quaid et al. | Jun 1992 | A |
5126618 | Takahashi et al. | Jun 1992 | A |
D327872 | McMills et al. | Jul 1992 | S |
5152762 | McElhenney | Oct 1992 | A |
5156633 | Smith | Oct 1992 | A |
5160334 | Billings et al. | Nov 1992 | A |
5162044 | Gahn et al. | Nov 1992 | A |
5163421 | Bernstein et al. | Nov 1992 | A |
5163537 | Radev | Nov 1992 | A |
5163945 | Ortiz et al. | Nov 1992 | A |
5167619 | Wuchinich | Dec 1992 | A |
5167725 | Clark et al. | Dec 1992 | A |
5172344 | Ehrlich | Dec 1992 | A |
5174276 | Crockard | Dec 1992 | A |
D332660 | Rawson et al. | Jan 1993 | S |
5176677 | Wuchinich | Jan 1993 | A |
5176695 | Dulebohn | Jan 1993 | A |
5184605 | Grzeszykowski | Feb 1993 | A |
5188102 | Idemoto et al. | Feb 1993 | A |
D334173 | Liu et al. | Mar 1993 | S |
5190517 | Zieve et al. | Mar 1993 | A |
5190541 | Abele et al. | Mar 1993 | A |
5196007 | Ellman et al. | Mar 1993 | A |
5205459 | Brinkerhoff et al. | Apr 1993 | A |
5209719 | Baruch et al. | May 1993 | A |
5213569 | Davis | May 1993 | A |
5214339 | Naito | May 1993 | A |
5217460 | Knoepfler | Jun 1993 | A |
5218529 | Meyer et al. | Jun 1993 | A |
5221282 | Wuchinich | Jun 1993 | A |
5222937 | Kagawa | Jun 1993 | A |
5226909 | Evans et al. | Jul 1993 | A |
5226910 | Kajiyama et al. | Jul 1993 | A |
5231989 | Middleman et al. | Aug 1993 | A |
5234428 | Kaufman | Aug 1993 | A |
5241236 | Sasaki et al. | Aug 1993 | A |
5241968 | Slater | Sep 1993 | A |
5242339 | Thornton | Sep 1993 | A |
5242460 | Klein et al. | Sep 1993 | A |
5246003 | DeLonzor | Sep 1993 | A |
5254129 | Alexander | Oct 1993 | A |
5257988 | L'Esperance, Jr. | Nov 1993 | A |
5258006 | Rydell et al. | Nov 1993 | A |
5261922 | Hood | Nov 1993 | A |
5263957 | Davison | Nov 1993 | A |
5264925 | Shipp et al. | Nov 1993 | A |
5275166 | Vaitekunas et al. | Jan 1994 | A |
5275607 | Lo et al. | Jan 1994 | A |
5275609 | Pingleton et al. | Jan 1994 | A |
5282800 | Foshee et al. | Feb 1994 | A |
5282817 | Hoogeboom et al. | Feb 1994 | A |
5285795 | Ryan et al. | Feb 1994 | A |
5285945 | Brinkerhoff et al. | Feb 1994 | A |
5290286 | Parins | Mar 1994 | A |
5300068 | Rosar et al. | Apr 1994 | A |
5304115 | Pflueger et al. | Apr 1994 | A |
D347474 | Olson | May 1994 | S |
5307976 | Olson et al. | May 1994 | A |
5309927 | Welch | May 1994 | A |
5312023 | Green et al. | May 1994 | A |
5312425 | Evans et al. | May 1994 | A |
5318563 | Malis et al. | Jun 1994 | A |
5318564 | Eggers | Jun 1994 | A |
5318589 | Lichtman | Jun 1994 | A |
5322055 | Davison et al. | Jun 1994 | A |
5324299 | Davison et al. | Jun 1994 | A |
5326013 | Green et al. | Jul 1994 | A |
5326342 | Pflueger et al. | Jul 1994 | A |
5330471 | Eggers | Jul 1994 | A |
5330502 | Hassler et al. | Jul 1994 | A |
5339723 | Huitema | Aug 1994 | A |
5342356 | Ellman et al. | Aug 1994 | A |
5342359 | Rydell | Aug 1994 | A |
5344420 | Hilal et al. | Sep 1994 | A |
5345937 | Middleman et al. | Sep 1994 | A |
5346502 | Estabrook et al. | Sep 1994 | A |
5353474 | Good et al. | Oct 1994 | A |
5357164 | Imabayashi et al. | Oct 1994 | A |
5357423 | Weaver et al. | Oct 1994 | A |
5359994 | Krauter et al. | Nov 1994 | A |
5361583 | Huitema | Nov 1994 | A |
5366466 | Christian et al. | Nov 1994 | A |
5368557 | Nita et al. | Nov 1994 | A |
5370645 | Klicek et al. | Dec 1994 | A |
5371429 | Manna | Dec 1994 | A |
5374813 | Shipp | Dec 1994 | A |
D354564 | Medema | Jan 1995 | S |
5381067 | Greenstein et al. | Jan 1995 | A |
5383874 | Jackson et al. | Jan 1995 | A |
5387207 | Dyer et al. | Feb 1995 | A |
5387215 | Fisher | Feb 1995 | A |
5389098 | Tsuruta et al. | Feb 1995 | A |
5394187 | Shipp | Feb 1995 | A |
5395312 | Desai | Mar 1995 | A |
5395363 | Billings et al. | Mar 1995 | A |
5395364 | Anderhub et al. | Mar 1995 | A |
5396266 | Brimhall | Mar 1995 | A |
5396900 | Slater et al. | Mar 1995 | A |
5400267 | Denen et al. | Mar 1995 | A |
5403312 | Yates et al. | Apr 1995 | A |
5403334 | Evans et al. | Apr 1995 | A |
5408268 | Shipp | Apr 1995 | A |
D358887 | Feinberg | May 1995 | S |
5411481 | Allen et al. | May 1995 | A |
5417709 | Slater | May 1995 | A |
5419761 | Narayanan et al. | May 1995 | A |
5421829 | Olichney et al. | Jun 1995 | A |
5423844 | Miller | Jun 1995 | A |
5428504 | Bhatla | Jun 1995 | A |
5429131 | Scheinman et al. | Jul 1995 | A |
5438997 | Sieben et al. | Aug 1995 | A |
5441499 | Fritzsch | Aug 1995 | A |
5443463 | Stern et al. | Aug 1995 | A |
5445638 | Rydell et al. | Aug 1995 | A |
5445639 | Kuslich et al. | Aug 1995 | A |
5449370 | Vaitekunas | Sep 1995 | A |
5451053 | Garrido | Sep 1995 | A |
5451220 | Ciervo | Sep 1995 | A |
5451227 | Michaelson | Sep 1995 | A |
5456684 | Schmidt et al. | Oct 1995 | A |
5458598 | Feinberg et al. | Oct 1995 | A |
5465895 | Knodel et al. | Nov 1995 | A |
5471988 | Fujio et al. | Dec 1995 | A |
5472443 | Cordis et al. | Dec 1995 | A |
5476479 | Green et al. | Dec 1995 | A |
5478003 | Green et al. | Dec 1995 | A |
5480409 | Riza | Jan 1996 | A |
5483501 | Park et al. | Jan 1996 | A |
5484436 | Eggers et al. | Jan 1996 | A |
5486162 | Brumbach | Jan 1996 | A |
5486189 | Mudry et al. | Jan 1996 | A |
5490860 | Middle et al. | Feb 1996 | A |
5496317 | Goble et al. | Mar 1996 | A |
5500216 | Julian et al. | Mar 1996 | A |
5501654 | Failla et al. | Mar 1996 | A |
5504650 | Katsui et al. | Apr 1996 | A |
5505693 | Mackool | Apr 1996 | A |
5507297 | Slater et al. | Apr 1996 | A |
5507738 | Ciervo | Apr 1996 | A |
5509922 | Aranyi et al. | Apr 1996 | A |
5511556 | DeSantis | Apr 1996 | A |
5520704 | Castro et al. | May 1996 | A |
5522839 | Pilling | Jun 1996 | A |
5527331 | Kresch et al. | Jun 1996 | A |
5531744 | Nardella et al. | Jul 1996 | A |
5540681 | Strul et al. | Jul 1996 | A |
5540693 | Fisher | Jul 1996 | A |
5542916 | Hirsch et al. | Aug 1996 | A |
5548286 | Craven | Aug 1996 | A |
5549637 | Crainich | Aug 1996 | A |
5553675 | Pitzen et al. | Sep 1996 | A |
5558671 | Yates | Sep 1996 | A |
5562609 | Brumbach | Oct 1996 | A |
5562610 | Brumbach | Oct 1996 | A |
5562659 | Morris | Oct 1996 | A |
5563179 | Stone et al. | Oct 1996 | A |
5569164 | Lurz | Oct 1996 | A |
5571121 | Heifetz | Nov 1996 | A |
5573424 | Poppe | Nov 1996 | A |
5573534 | Stone | Nov 1996 | A |
5577654 | Bishop | Nov 1996 | A |
5584830 | Ladd et al. | Dec 1996 | A |
5591187 | Dekel | Jan 1997 | A |
5593414 | Shipp et al. | Jan 1997 | A |
5599350 | Schulze et al. | Feb 1997 | A |
5600526 | Russell et al. | Feb 1997 | A |
5601601 | Tal et al. | Feb 1997 | A |
5603773 | Campbell | Feb 1997 | A |
5607436 | Pratt et al. | Mar 1997 | A |
5607450 | Zvenyatsky et al. | Mar 1997 | A |
5609573 | Sandock | Mar 1997 | A |
5611813 | Lichtman | Mar 1997 | A |
5618304 | Hart et al. | Apr 1997 | A |
5618307 | Donlon et al. | Apr 1997 | A |
5618492 | Auten et al. | Apr 1997 | A |
5620447 | Smith et al. | Apr 1997 | A |
5624452 | Yates | Apr 1997 | A |
5626587 | Bishop et al. | May 1997 | A |
5626595 | Sklar et al. | May 1997 | A |
5628760 | Knoepfler | May 1997 | A |
5630420 | Vaitekunas | May 1997 | A |
5632432 | Schulze et al. | May 1997 | A |
5632717 | Yoon | May 1997 | A |
5640741 | Yano | Jun 1997 | A |
D381077 | Hunt | Jul 1997 | S |
5647871 | Levine et al. | Jul 1997 | A |
5649937 | Bito et al. | Jul 1997 | A |
5651780 | Jackson et al. | Jul 1997 | A |
5653713 | Michelson | Aug 1997 | A |
5655100 | Ebrahim et al. | Aug 1997 | A |
5658281 | Heard | Aug 1997 | A |
5662662 | Bishop et al. | Sep 1997 | A |
5662667 | Knodel | Sep 1997 | A |
5665085 | Nardella | Sep 1997 | A |
5665100 | Yoon | Sep 1997 | A |
5669922 | Hood | Sep 1997 | A |
5674219 | Monson et al. | Oct 1997 | A |
5674220 | Fox et al. | Oct 1997 | A |
5674235 | Parisi | Oct 1997 | A |
5678568 | Uchikubo et al. | Oct 1997 | A |
5688270 | Yates et al. | Nov 1997 | A |
5690269 | Bolanos et al. | Nov 1997 | A |
5693051 | Schulze et al. | Dec 1997 | A |
5694936 | Fujimoto et al. | Dec 1997 | A |
5695510 | Hood | Dec 1997 | A |
5700261 | Brinkerhoff | Dec 1997 | A |
5704534 | Huitema et al. | Jan 1998 | A |
5707369 | Vaitekunas et al. | Jan 1998 | A |
5709680 | Yates et al. | Jan 1998 | A |
5711472 | Bryan | Jan 1998 | A |
5713896 | Nardella | Feb 1998 | A |
5715817 | Stevens-Wright et al. | Feb 1998 | A |
5716366 | Yates | Feb 1998 | A |
5717306 | Shipp | Feb 1998 | A |
5720742 | Zacharias | Feb 1998 | A |
5720744 | Eggleston et al. | Feb 1998 | A |
5723970 | Bell | Mar 1998 | A |
5728130 | Ishikawa et al. | Mar 1998 | A |
5730752 | Alden et al. | Mar 1998 | A |
5733074 | Stock et al. | Mar 1998 | A |
5735848 | Yates et al. | Apr 1998 | A |
5741226 | Strukel et al. | Apr 1998 | A |
5743906 | Parins et al. | Apr 1998 | A |
5752973 | Kieturakis | May 1998 | A |
5755717 | Yates et al. | May 1998 | A |
5762255 | Chrisman et al. | Jun 1998 | A |
5766164 | Mueller et al. | Jun 1998 | A |
5772659 | Becker et al. | Jun 1998 | A |
5776155 | Beaupre et al. | Jul 1998 | A |
5779701 | McBrayer et al. | Jul 1998 | A |
5782834 | Lucey et al. | Jul 1998 | A |
5792135 | Madhani et al. | Aug 1998 | A |
5792138 | Shipp | Aug 1998 | A |
5792165 | Klieman et al. | Aug 1998 | A |
5796188 | Bays | Aug 1998 | A |
5797941 | Schulze et al. | Aug 1998 | A |
5797958 | Yoon | Aug 1998 | A |
5797959 | Castro et al. | Aug 1998 | A |
5800432 | Swanson | Sep 1998 | A |
5800448 | Banko | Sep 1998 | A |
5800449 | Wales | Sep 1998 | A |
5805140 | Rosenberg et al. | Sep 1998 | A |
5807393 | Williamson, IV et al. | Sep 1998 | A |
5808396 | Boukhny | Sep 1998 | A |
5810811 | Yates et al. | Sep 1998 | A |
5810859 | DiMatteo et al. | Sep 1998 | A |
5817033 | DeSantis et al. | Oct 1998 | A |
5817084 | Jensen | Oct 1998 | A |
5817093 | Williamson, IV et al. | Oct 1998 | A |
5817119 | Klieman et al. | Oct 1998 | A |
5823197 | Edwards | Oct 1998 | A |
5827271 | Buysse et al. | Oct 1998 | A |
5827323 | Klieman et al. | Oct 1998 | A |
5828160 | Sugishita | Oct 1998 | A |
5833696 | Whitfield et al. | Nov 1998 | A |
5836897 | Sakurai et al. | Nov 1998 | A |
5836909 | Cosmescu | Nov 1998 | A |
5836943 | Miller, III | Nov 1998 | A |
5836957 | Schulz et al. | Nov 1998 | A |
5836990 | Li | Nov 1998 | A |
5843109 | Mehta et al. | Dec 1998 | A |
5851212 | Zirps et al. | Dec 1998 | A |
5853412 | Mayenberger | Dec 1998 | A |
5858018 | Shipp et al. | Jan 1999 | A |
5865361 | Milliman et al. | Feb 1999 | A |
5873873 | Smith et al. | Feb 1999 | A |
5873882 | Straub et al. | Feb 1999 | A |
5876401 | Schulze et al. | Mar 1999 | A |
5878193 | Wang et al. | Mar 1999 | A |
5879364 | Bromfield et al. | Mar 1999 | A |
5880668 | Hall | Mar 1999 | A |
5883615 | Fago et al. | Mar 1999 | A |
5891142 | Eggers et al. | Apr 1999 | A |
5893835 | Witt et al. | Apr 1999 | A |
5897523 | Wright et al. | Apr 1999 | A |
5897569 | Kellogg et al. | Apr 1999 | A |
5903607 | Tailliet | May 1999 | A |
5904681 | West, Jr. | May 1999 | A |
5906625 | Bito et al. | May 1999 | A |
5906627 | Spaulding | May 1999 | A |
5906628 | Miyawaki et al. | May 1999 | A |
5910129 | Koblish et al. | Jun 1999 | A |
5911699 | Anis et al. | Jun 1999 | A |
5913823 | Hedberg et al. | Jun 1999 | A |
5916229 | Evans | Jun 1999 | A |
5921956 | Grinberg et al. | Jul 1999 | A |
5929846 | Rosenberg et al. | Jul 1999 | A |
5935143 | Hood | Aug 1999 | A |
5935144 | Estabrook | Aug 1999 | A |
5938633 | Beaupre | Aug 1999 | A |
5944718 | Austin et al. | Aug 1999 | A |
5944737 | Tsonton et al. | Aug 1999 | A |
5947984 | Whipple | Sep 1999 | A |
5954717 | Behl et al. | Sep 1999 | A |
5954736 | Bishop et al. | Sep 1999 | A |
5954746 | Holthaus et al. | Sep 1999 | A |
5957882 | Nita et al. | Sep 1999 | A |
5957943 | Vaitekunas | Sep 1999 | A |
5968007 | Simon et al. | Oct 1999 | A |
5968060 | Kellogg | Oct 1999 | A |
5974342 | Petrofsky | Oct 1999 | A |
D416089 | Barton et al. | Nov 1999 | S |
5980510 | Tsonton et al. | Nov 1999 | A |
5980546 | Hood | Nov 1999 | A |
5984938 | Yoon | Nov 1999 | A |
5989274 | Davison et al. | Nov 1999 | A |
5989275 | Estabrook et al. | Nov 1999 | A |
5993465 | Shipp et al. | Nov 1999 | A |
5993972 | Reich et al. | Nov 1999 | A |
5994855 | Lundell et al. | Nov 1999 | A |
6003517 | Sheffield et al. | Dec 1999 | A |
6013052 | Durman et al. | Jan 2000 | A |
6024741 | Williamson, IV et al. | Feb 2000 | A |
6024744 | Kese et al. | Feb 2000 | A |
6024750 | Mastri et al. | Feb 2000 | A |
6027515 | Cimino | Feb 2000 | A |
6031526 | Shipp | Feb 2000 | A |
6033375 | Brumbach | Mar 2000 | A |
6033399 | Gines | Mar 2000 | A |
6036667 | Manna et al. | Mar 2000 | A |
6036707 | Spaulding | Mar 2000 | A |
6039734 | Goble | Mar 2000 | A |
6048224 | Kay | Apr 2000 | A |
6050943 | Slayton et al. | Apr 2000 | A |
6050996 | Schmaltz et al. | Apr 2000 | A |
6051010 | DiMatteo et al. | Apr 2000 | A |
6056735 | Okada et al. | May 2000 | A |
6063098 | Houser et al. | May 2000 | A |
6066132 | Chen et al. | May 2000 | A |
6066151 | Miyawaki et al. | May 2000 | A |
6068627 | Orszulak et al. | May 2000 | A |
6068629 | Haissaguerre et al. | May 2000 | A |
6068647 | Witt et al. | May 2000 | A |
6074389 | Levine et al. | Jun 2000 | A |
6077285 | Boukhny | Jun 2000 | A |
6080149 | Huang et al. | Jun 2000 | A |
6083191 | Rose | Jul 2000 | A |
6086584 | Miller | Jul 2000 | A |
6090120 | Wright et al. | Jul 2000 | A |
6091995 | Ingle et al. | Jul 2000 | A |
6096033 | Tu et al. | Aug 2000 | A |
6099483 | Palmer et al. | Aug 2000 | A |
6099542 | Cohn et al. | Aug 2000 | A |
6099550 | Yoon | Aug 2000 | A |
6109500 | Alli et al. | Aug 2000 | A |
6110127 | Suzuki | Aug 2000 | A |
6113594 | Savage | Sep 2000 | A |
6117152 | Huitema | Sep 2000 | A |
H001904 | Yates et al. | Oct 2000 | H |
6126629 | Perkins | Oct 2000 | A |
6126658 | Baker | Oct 2000 | A |
6129735 | Okada et al. | Oct 2000 | A |
6129740 | Michelson | Oct 2000 | A |
6132368 | Cooper | Oct 2000 | A |
6132427 | Jones et al. | Oct 2000 | A |
6132429 | Baker | Oct 2000 | A |
6132448 | Perez et al. | Oct 2000 | A |
6139320 | Hahn | Oct 2000 | A |
6139561 | Shibata et al. | Oct 2000 | A |
6142615 | Qiu et al. | Nov 2000 | A |
6142994 | Swanson et al. | Nov 2000 | A |
6144402 | Norsworthy et al. | Nov 2000 | A |
6147560 | Erhage et al. | Nov 2000 | A |
6152902 | Christian et al. | Nov 2000 | A |
6152923 | Ryan | Nov 2000 | A |
6154198 | Rosenberg | Nov 2000 | A |
6159160 | Hsei et al. | Dec 2000 | A |
6159175 | Strukel et al. | Dec 2000 | A |
6162194 | Shipp | Dec 2000 | A |
6162208 | Hipps | Dec 2000 | A |
6165150 | Banko | Dec 2000 | A |
6174309 | Wrublewski et al. | Jan 2001 | B1 |
6174310 | Kirwan, Jr. | Jan 2001 | B1 |
6176857 | Ashley | Jan 2001 | B1 |
6179853 | Sachse et al. | Jan 2001 | B1 |
6183426 | Akisada et al. | Feb 2001 | B1 |
6187003 | Buysse et al. | Feb 2001 | B1 |
6190386 | Rydell | Feb 2001 | B1 |
6193709 | Miyawaki et al. | Feb 2001 | B1 |
6204592 | Hur | Mar 2001 | B1 |
6205855 | Pfeiffer | Mar 2001 | B1 |
6206844 | Reichel et al. | Mar 2001 | B1 |
6206876 | Levine et al. | Mar 2001 | B1 |
6210337 | Dunham et al. | Apr 2001 | B1 |
6210402 | Olsen et al. | Apr 2001 | B1 |
6210403 | Klicek | Apr 2001 | B1 |
6214023 | Whipple et al. | Apr 2001 | B1 |
6228080 | Gines | May 2001 | B1 |
6231565 | Tovey et al. | May 2001 | B1 |
6233476 | Strommer et al. | May 2001 | B1 |
6238366 | Savage et al. | May 2001 | B1 |
6245065 | Panescu et al. | Jun 2001 | B1 |
6251110 | Wampler | Jun 2001 | B1 |
6252110 | Uemura et al. | Jun 2001 | B1 |
D444365 | Bass et al. | Jul 2001 | S |
D445092 | Lee | Jul 2001 | S |
D445764 | Lee | Jul 2001 | S |
6254623 | Haibel, Jr. et al. | Jul 2001 | B1 |
6257241 | Wampler | Jul 2001 | B1 |
6258034 | Hanafy | Jul 2001 | B1 |
6259230 | Chou | Jul 2001 | B1 |
6267761 | Ryan | Jul 2001 | B1 |
6270831 | Kumar et al. | Aug 2001 | B2 |
6273852 | Lehe et al. | Aug 2001 | B1 |
6274963 | Estabrook et al. | Aug 2001 | B1 |
6277115 | Saadat | Aug 2001 | B1 |
6277117 | Tetzlaff et al. | Aug 2001 | B1 |
6278218 | Madan et al. | Aug 2001 | B1 |
6280407 | Manna et al. | Aug 2001 | B1 |
6283981 | Beaupre | Sep 2001 | B1 |
6287344 | Wampler et al. | Sep 2001 | B1 |
6290575 | Shipp | Sep 2001 | B1 |
6292700 | Morrison et al. | Sep 2001 | B1 |
6299591 | Banko | Oct 2001 | B1 |
6306131 | Hareyama et al. | Oct 2001 | B1 |
6306157 | Shchervinsky | Oct 2001 | B1 |
6309400 | Beaupre | Oct 2001 | B2 |
6311783 | Harpell | Nov 2001 | B1 |
6319221 | Savage et al. | Nov 2001 | B1 |
6325795 | Lindemann et al. | Dec 2001 | B1 |
6325799 | Goble | Dec 2001 | B1 |
6325811 | Messerly | Dec 2001 | B1 |
6328751 | Beaupre | Dec 2001 | B1 |
6332891 | Himes | Dec 2001 | B1 |
6338657 | Harper et al. | Jan 2002 | B1 |
6340352 | Okada et al. | Jan 2002 | B1 |
6340878 | Oglesbee | Jan 2002 | B1 |
6350269 | Shipp et al. | Feb 2002 | B1 |
6352532 | Kramer et al. | Mar 2002 | B1 |
6356224 | Wohlfarth | Mar 2002 | B1 |
6358246 | Behl et al. | Mar 2002 | B1 |
6358264 | Banko | Mar 2002 | B2 |
6364888 | Niemeyer et al. | Apr 2002 | B1 |
6379320 | Lafon et al. | Apr 2002 | B1 |
D457958 | Dycus et al. | May 2002 | S |
6383194 | Pothula | May 2002 | B1 |
6384690 | Wilhelmsson et al. | May 2002 | B1 |
6387109 | Davison et al. | May 2002 | B1 |
6388657 | Natoli | May 2002 | B1 |
6390973 | Ouchi | May 2002 | B1 |
6391026 | Hung et al. | May 2002 | B1 |
6391042 | Cimino | May 2002 | B1 |
6398779 | Buysse et al. | Jun 2002 | B1 |
6402743 | Orszulak et al. | Jun 2002 | B1 |
6402748 | Schoenman et al. | Jun 2002 | B1 |
6405733 | Fogarty et al. | Jun 2002 | B1 |
6409722 | Hoey et al. | Jun 2002 | B1 |
H002037 | Yates et al. | Jul 2002 | H |
6416486 | Wampler | Jul 2002 | B1 |
6419675 | Gallo, Sr. | Jul 2002 | B1 |
6423073 | Bowman | Jul 2002 | B2 |
6423082 | Houser et al. | Jul 2002 | B1 |
6425906 | Young et al. | Jul 2002 | B1 |
6428538 | Blewett et al. | Aug 2002 | B1 |
6428539 | Baxter et al. | Aug 2002 | B1 |
6430446 | Knowlton | Aug 2002 | B1 |
6432118 | Messerly | Aug 2002 | B1 |
6436114 | Novak et al. | Aug 2002 | B1 |
6436115 | Beaupre | Aug 2002 | B1 |
6440062 | Ouchi | Aug 2002 | B1 |
6443968 | Holthaus et al. | Sep 2002 | B1 |
6443969 | Novak et al. | Sep 2002 | B1 |
6449006 | Shipp | Sep 2002 | B1 |
6454781 | Witt et al. | Sep 2002 | B1 |
6454782 | Schwemberger | Sep 2002 | B1 |
6458128 | Schulze | Oct 2002 | B1 |
6458142 | Faller et al. | Oct 2002 | B1 |
6459363 | Walker et al. | Oct 2002 | B1 |
6464689 | Qin et al. | Oct 2002 | B1 |
6464702 | Schulze et al. | Oct 2002 | B2 |
6468270 | Hovda et al. | Oct 2002 | B1 |
6475215 | Tanrisever | Nov 2002 | B1 |
6480796 | Wiener | Nov 2002 | B2 |
6485490 | Wampler et al. | Nov 2002 | B2 |
6491690 | Goble et al. | Dec 2002 | B1 |
6491701 | Tierney et al. | Dec 2002 | B2 |
6491708 | Madan et al. | Dec 2002 | B2 |
6497715 | Satou | Dec 2002 | B2 |
6500112 | Khouri | Dec 2002 | B1 |
6500176 | Truckai et al. | Dec 2002 | B1 |
6500188 | Harper et al. | Dec 2002 | B2 |
6500312 | Wedekamp | Dec 2002 | B2 |
6503248 | Levine | Jan 2003 | B1 |
6506208 | Hunt et al. | Jan 2003 | B2 |
6511478 | Burnside et al. | Jan 2003 | B1 |
6511480 | Tetzlaff et al. | Jan 2003 | B1 |
6511493 | Moutafis et al. | Jan 2003 | B1 |
6514252 | Nezhat et al. | Feb 2003 | B2 |
6514267 | Jewett | Feb 2003 | B2 |
6517565 | Whitman et al. | Feb 2003 | B1 |
6524251 | Rabiner et al. | Feb 2003 | B2 |
6524316 | Nicholson et al. | Feb 2003 | B1 |
6527736 | Attinger et al. | Mar 2003 | B1 |
6531846 | Smith | Mar 2003 | B1 |
6533784 | Truckai et al. | Mar 2003 | B2 |
6537272 | Christopherson et al. | Mar 2003 | B2 |
6537291 | Friedman et al. | Mar 2003 | B2 |
6543452 | Lavigne | Apr 2003 | B1 |
6543456 | Freeman | Apr 2003 | B1 |
6544260 | Markel et al. | Apr 2003 | B1 |
6551309 | LePivert | Apr 2003 | B1 |
6554829 | Schulze et al. | Apr 2003 | B2 |
6558376 | Bishop | May 2003 | B2 |
6561983 | Cronin et al. | May 2003 | B2 |
6562035 | Levin | May 2003 | B1 |
6562037 | Paton et al. | May 2003 | B2 |
6565558 | Lindenmeier et al. | May 2003 | B1 |
6572563 | Ouchi | Jun 2003 | B2 |
6572632 | Zisterer et al. | Jun 2003 | B2 |
6572639 | Ingle et al. | Jun 2003 | B1 |
6575969 | Rittman, III et al. | Jun 2003 | B1 |
6582427 | Goble et al. | Jun 2003 | B1 |
6582451 | Marucci et al. | Jun 2003 | B1 |
6584360 | Francischelli et al. | Jun 2003 | B2 |
D477408 | Bromley | Jul 2003 | S |
6585735 | Frazier et al. | Jul 2003 | B1 |
6588277 | Giordano et al. | Jul 2003 | B2 |
6589200 | Schwemberger et al. | Jul 2003 | B1 |
6589239 | Khandkar et al. | Jul 2003 | B2 |
6590733 | Wilson et al. | Jul 2003 | B1 |
6599288 | Maguire et al. | Jul 2003 | B2 |
6602252 | Mollenauer | Aug 2003 | B2 |
6607540 | Shipp | Aug 2003 | B1 |
6610059 | West, Jr. | Aug 2003 | B1 |
6610060 | Mulier et al. | Aug 2003 | B2 |
6611793 | Burnside et al. | Aug 2003 | B1 |
6616450 | Mossle et al. | Sep 2003 | B2 |
6619529 | Green et al. | Sep 2003 | B2 |
6620161 | Schulze et al. | Sep 2003 | B2 |
6622731 | Daniel et al. | Sep 2003 | B2 |
6623482 | Pendekanti et al. | Sep 2003 | B2 |
6623500 | Cook et al. | Sep 2003 | B1 |
6623501 | Heller et al. | Sep 2003 | B2 |
6626848 | Neuenfeldt | Sep 2003 | B2 |
6626926 | Friedman et al. | Sep 2003 | B2 |
6629974 | Penny et al. | Oct 2003 | B2 |
6633234 | Wiener et al. | Oct 2003 | B2 |
6635057 | Harano et al. | Oct 2003 | B2 |
6644532 | Green et al. | Nov 2003 | B2 |
6651669 | Burnside | Nov 2003 | B1 |
6652513 | Panescu et al. | Nov 2003 | B2 |
6652539 | Shipp et al. | Nov 2003 | B2 |
6652545 | Shipp et al. | Nov 2003 | B2 |
6656132 | Ouchi | Dec 2003 | B1 |
6656177 | Truckai et al. | Dec 2003 | B2 |
6656198 | Tsonton et al. | Dec 2003 | B2 |
6660017 | Beaupre | Dec 2003 | B2 |
6662127 | Wiener et al. | Dec 2003 | B2 |
6663941 | Brown et al. | Dec 2003 | B2 |
6666860 | Takahashi | Dec 2003 | B1 |
6666875 | Sakurai et al. | Dec 2003 | B1 |
6669690 | Okada et al. | Dec 2003 | B1 |
6669710 | Moutafis et al. | Dec 2003 | B2 |
6673248 | Chowdhury | Jan 2004 | B2 |
6676660 | Wampler et al. | Jan 2004 | B2 |
6678621 | Wiener et al. | Jan 2004 | B2 |
6679875 | Honda et al. | Jan 2004 | B2 |
6679882 | Kornerup | Jan 2004 | B1 |
6679899 | Wiener et al. | Jan 2004 | B2 |
6682501 | Nelson et al. | Jan 2004 | B1 |
6682544 | Mastri et al. | Jan 2004 | B2 |
6685700 | Behl et al. | Feb 2004 | B2 |
6685701 | Orszulak et al. | Feb 2004 | B2 |
6685703 | Pearson et al. | Feb 2004 | B2 |
6689145 | Lee et al. | Feb 2004 | B2 |
6689146 | Himes | Feb 2004 | B1 |
6690960 | Chen et al. | Feb 2004 | B2 |
6695840 | Schulze | Feb 2004 | B2 |
6702821 | Bonutti | Mar 2004 | B2 |
6716215 | David et al. | Apr 2004 | B1 |
6719692 | Kleffner et al. | Apr 2004 | B2 |
6719765 | Bonutti | Apr 2004 | B2 |
6719776 | Baxter et al. | Apr 2004 | B2 |
6722552 | Fenton, Jr. | Apr 2004 | B2 |
6723091 | Goble et al. | Apr 2004 | B2 |
D490059 | Conway et al. | May 2004 | S |
6731047 | Kauf et al. | May 2004 | B2 |
6733498 | Paton et al. | May 2004 | B2 |
6733506 | McDevitt et al. | May 2004 | B1 |
6736813 | Yamauchi et al. | May 2004 | B2 |
6739872 | Turri | May 2004 | B1 |
6740079 | Eggers et al. | May 2004 | B1 |
D491666 | Kimmell et al. | Jun 2004 | S |
6743245 | Lobdell | Jun 2004 | B2 |
6746284 | Spink, Jr. | Jun 2004 | B1 |
6746443 | Morley et al. | Jun 2004 | B1 |
6752815 | Beaupre | Jun 2004 | B2 |
6755825 | Shoenman et al. | Jun 2004 | B2 |
6761698 | Shibata et al. | Jul 2004 | B2 |
6762535 | Take et al. | Jul 2004 | B2 |
6766202 | Underwood et al. | Jul 2004 | B2 |
6770072 | Truckai et al. | Aug 2004 | B1 |
6773409 | Truckai et al. | Aug 2004 | B2 |
6773435 | Schulze et al. | Aug 2004 | B2 |
6773443 | Truwit et al. | Aug 2004 | B2 |
6773444 | Messerly | Aug 2004 | B2 |
6775575 | Bommannan et al. | Aug 2004 | B2 |
6778023 | Christensen | Aug 2004 | B2 |
6783524 | Anderson et al. | Aug 2004 | B2 |
6786382 | Hoffman | Sep 2004 | B1 |
6786383 | Stegelmann | Sep 2004 | B2 |
6789939 | Schrodinger et al. | Sep 2004 | B2 |
6790173 | Saadat et al. | Sep 2004 | B2 |
6790216 | Ishikawa | Sep 2004 | B1 |
6794027 | Araki et al. | Sep 2004 | B1 |
6796981 | Wham et al. | Sep 2004 | B2 |
D496997 | Dycus et al. | Oct 2004 | S |
6800085 | Selmon et al. | Oct 2004 | B2 |
6802843 | Truckai et al. | Oct 2004 | B2 |
6808525 | Latterell et al. | Oct 2004 | B2 |
6809508 | Donofrio | Oct 2004 | B2 |
6810281 | Brock et al. | Oct 2004 | B2 |
6811842 | Ehrnsperger et al. | Nov 2004 | B1 |
6814731 | Swanson | Nov 2004 | B2 |
6819027 | Saraf | Nov 2004 | B2 |
6821273 | Mollenauer | Nov 2004 | B2 |
6827712 | Tovey et al. | Dec 2004 | B2 |
6828712 | Battaglin et al. | Dec 2004 | B2 |
6835082 | Gonnering | Dec 2004 | B2 |
6835199 | McGuckin, Jr. et al. | Dec 2004 | B2 |
6840938 | Morley et al. | Jan 2005 | B1 |
6843789 | Goble | Jan 2005 | B2 |
6849073 | Hoey et al. | Feb 2005 | B2 |
6860878 | Brock | Mar 2005 | B2 |
6860880 | Treat et al. | Mar 2005 | B2 |
6863676 | Lee et al. | Mar 2005 | B2 |
6866671 | Tierney et al. | Mar 2005 | B2 |
6869439 | White et al. | Mar 2005 | B2 |
6875220 | Du et al. | Apr 2005 | B2 |
6877647 | Green et al. | Apr 2005 | B2 |
6882439 | Ishijima | Apr 2005 | B2 |
6887209 | Kadziauskas et al. | May 2005 | B2 |
6887252 | Okada et al. | May 2005 | B1 |
6893435 | Goble | May 2005 | B2 |
6898536 | Wiener et al. | May 2005 | B2 |
6899685 | Kermode et al. | May 2005 | B2 |
6905497 | Truckai et al. | Jun 2005 | B2 |
6908463 | Treat et al. | Jun 2005 | B2 |
6908472 | Wiener et al. | Jun 2005 | B2 |
6913579 | Truckai et al. | Jul 2005 | B2 |
6915623 | Dey et al. | Jul 2005 | B2 |
6923804 | Eggers et al. | Aug 2005 | B2 |
6923806 | Hooven et al. | Aug 2005 | B2 |
6926712 | Phan | Aug 2005 | B2 |
6926716 | Baker et al. | Aug 2005 | B2 |
6926717 | Garito et al. | Aug 2005 | B1 |
6929602 | Hirakui et al. | Aug 2005 | B2 |
6929622 | Chian | Aug 2005 | B2 |
6929632 | Nita et al. | Aug 2005 | B2 |
6929644 | Truckai et al. | Aug 2005 | B2 |
6933656 | Matsushita et al. | Aug 2005 | B2 |
D509589 | Wells | Sep 2005 | S |
6942660 | Pantera et al. | Sep 2005 | B2 |
6942677 | Nita et al. | Sep 2005 | B2 |
6945981 | Donofrio et al. | Sep 2005 | B2 |
6946779 | Birgel | Sep 2005 | B2 |
6948503 | Refior et al. | Sep 2005 | B2 |
6953461 | McClurken et al. | Oct 2005 | B2 |
D511145 | Donofrio et al. | Nov 2005 | S |
6974450 | Weber et al. | Dec 2005 | B2 |
6976844 | Hickok et al. | Dec 2005 | B2 |
6976969 | Messerly | Dec 2005 | B2 |
6977495 | Donofrio | Dec 2005 | B2 |
6979332 | Adams | Dec 2005 | B2 |
6981628 | Wales | Jan 2006 | B2 |
6984220 | Wuchinich | Jan 2006 | B2 |
6988295 | Tillim | Jan 2006 | B2 |
6994708 | Manzo | Feb 2006 | B2 |
6994709 | Iida | Feb 2006 | B2 |
7000818 | Shelton, IV et al. | Feb 2006 | B2 |
7001335 | Adachi et al. | Feb 2006 | B2 |
7001379 | Behl et al. | Feb 2006 | B2 |
7001382 | Gallo, Sr. | Feb 2006 | B2 |
7011657 | Truckai et al. | Mar 2006 | B2 |
7014638 | Michelson | Mar 2006 | B2 |
7025732 | Thompson et al. | Apr 2006 | B2 |
7033356 | Latterell et al. | Apr 2006 | B2 |
7033357 | Baxter et al. | Apr 2006 | B2 |
7037306 | Podany et al. | May 2006 | B2 |
7041083 | Chu et al. | May 2006 | B2 |
7041088 | Nawrocki et al. | May 2006 | B2 |
7041102 | Truckai et al. | May 2006 | B2 |
7044949 | Orszulak et al. | May 2006 | B2 |
7052496 | Yamauchi | May 2006 | B2 |
7055731 | Shelton, IV et al. | Jun 2006 | B2 |
7063699 | Hess et al. | Jun 2006 | B2 |
7066893 | Hibner et al. | Jun 2006 | B2 |
7066895 | Podany | Jun 2006 | B2 |
7066936 | Ryan | Jun 2006 | B2 |
7070597 | Truckai et al. | Jul 2006 | B2 |
7074218 | Washington et al. | Jul 2006 | B2 |
7074219 | Levine et al. | Jul 2006 | B2 |
7077039 | Gass et al. | Jul 2006 | B2 |
7077845 | Hacker et al. | Jul 2006 | B2 |
7077853 | Kramer et al. | Jul 2006 | B2 |
7083613 | Treat | Aug 2006 | B2 |
7083618 | Couture et al. | Aug 2006 | B2 |
7083619 | Truckai et al. | Aug 2006 | B2 |
7087054 | Truckai et al. | Aug 2006 | B2 |
7090672 | Underwood et al. | Aug 2006 | B2 |
7094235 | Francischelli | Aug 2006 | B2 |
7101371 | Dycus et al. | Sep 2006 | B2 |
7101372 | Dycus et al. | Sep 2006 | B2 |
7101373 | Dycus et al. | Sep 2006 | B2 |
7101378 | Salameh et al. | Sep 2006 | B2 |
7104834 | Robinson et al. | Sep 2006 | B2 |
7108695 | Witt et al. | Sep 2006 | B2 |
7111769 | Wales et al. | Sep 2006 | B2 |
7112201 | Truckai et al. | Sep 2006 | B2 |
7113831 | Hooven | Sep 2006 | B2 |
D531311 | Guerra et al. | Oct 2006 | S |
7117034 | Kronberg | Oct 2006 | B2 |
7118564 | Ritchie et al. | Oct 2006 | B2 |
7118570 | Tetzlaff et al. | Oct 2006 | B2 |
7124932 | Isaacson et al. | Oct 2006 | B2 |
7125409 | Truckai et al. | Oct 2006 | B2 |
7128720 | Podany | Oct 2006 | B2 |
7131860 | Sartor et al. | Nov 2006 | B2 |
7131970 | Moses et al. | Nov 2006 | B2 |
7135018 | Ryan et al. | Nov 2006 | B2 |
7135030 | Schwemberger et al. | Nov 2006 | B2 |
7137980 | Buysse et al. | Nov 2006 | B2 |
7143925 | Shelton, IV et al. | Dec 2006 | B2 |
7144403 | Booth | Dec 2006 | B2 |
7147138 | Shelton, IV | Dec 2006 | B2 |
7153315 | Miller | Dec 2006 | B2 |
D536093 | Nakajima et al. | Jan 2007 | S |
7156189 | Bar-Cohen et al. | Jan 2007 | B1 |
7156846 | Dycus et al. | Jan 2007 | B2 |
7156853 | Muratsu | Jan 2007 | B2 |
7157058 | Marhasin et al. | Jan 2007 | B2 |
7159750 | Racenet et al. | Jan 2007 | B2 |
7160296 | Pearson et al. | Jan 2007 | B2 |
7160298 | Lawes et al. | Jan 2007 | B2 |
7160299 | Baily | Jan 2007 | B2 |
7163548 | Stulen et al. | Jan 2007 | B2 |
7169144 | Hoey et al. | Jan 2007 | B2 |
7169146 | Truckai et al. | Jan 2007 | B2 |
7169156 | Hart | Jan 2007 | B2 |
7179254 | Pendekanti et al. | Feb 2007 | B2 |
7179271 | Friedman et al. | Feb 2007 | B2 |
7186253 | Truckai et al. | Mar 2007 | B2 |
7189233 | Truckai et al. | Mar 2007 | B2 |
7195631 | Dumbauld | Mar 2007 | B2 |
D541418 | Schechter et al. | Apr 2007 | S |
7198635 | Danek et al. | Apr 2007 | B2 |
7204820 | Akahoshi | Apr 2007 | B2 |
7207471 | Heinrich et al. | Apr 2007 | B2 |
7207997 | Shipp et al. | Apr 2007 | B2 |
7210881 | Greenberg | May 2007 | B2 |
7211079 | Treat | May 2007 | B2 |
7217128 | Atkin et al. | May 2007 | B2 |
7217269 | El-Galley et al. | May 2007 | B2 |
7220951 | Truckai et al. | May 2007 | B2 |
7223229 | Inman et al. | May 2007 | B2 |
7225964 | Mastri et al. | Jun 2007 | B2 |
7226448 | Bertolero et al. | Jun 2007 | B2 |
7229455 | Sakurai et al. | Jun 2007 | B2 |
7232440 | Dumbauld et al. | Jun 2007 | B2 |
7235071 | Gonnering | Jun 2007 | B2 |
7235073 | Levine et al. | Jun 2007 | B2 |
7241294 | Reschke | Jul 2007 | B2 |
7244262 | Wiener et al. | Jul 2007 | B2 |
7251531 | Mosher et al. | Jul 2007 | B2 |
7252641 | Thompson et al. | Aug 2007 | B2 |
7252667 | Moses et al. | Aug 2007 | B2 |
7258688 | Shah et al. | Aug 2007 | B1 |
7267677 | Johnson et al. | Sep 2007 | B2 |
7267685 | Butaric et al. | Sep 2007 | B2 |
7269873 | Brewer et al. | Sep 2007 | B2 |
7273483 | Wiener et al. | Sep 2007 | B2 |
D552241 | Bromley et al. | Oct 2007 | S |
7282048 | Goble et al. | Oct 2007 | B2 |
7285895 | Beaupre | Oct 2007 | B2 |
7287682 | Ezzat et al. | Oct 2007 | B1 |
7297149 | Vitali et al. | Nov 2007 | B2 |
7300431 | Dubrovsky | Nov 2007 | B2 |
7300435 | Wham et al. | Nov 2007 | B2 |
7300446 | Beaupre | Nov 2007 | B2 |
7300450 | Vleugels et al. | Nov 2007 | B2 |
7303531 | Lee et al. | Dec 2007 | B2 |
7303557 | Wham et al. | Dec 2007 | B2 |
7306597 | Manzo | Dec 2007 | B2 |
7307313 | Ohyanagi et al. | Dec 2007 | B2 |
7309849 | Truckai et al. | Dec 2007 | B2 |
7311706 | Schoenman et al. | Dec 2007 | B2 |
7311709 | Truckai et al. | Dec 2007 | B2 |
7317955 | McGreevy | Jan 2008 | B2 |
7318831 | Alvarez et al. | Jan 2008 | B2 |
7326236 | Andreas et al. | Feb 2008 | B2 |
7329257 | Kanehira et al. | Feb 2008 | B2 |
7331410 | Yong et al. | Feb 2008 | B2 |
7335165 | Truwit et al. | Feb 2008 | B2 |
7335997 | Wiener | Feb 2008 | B2 |
7337010 | Howard et al. | Feb 2008 | B2 |
7353068 | Tanaka et al. | Apr 2008 | B2 |
7354440 | Truckal et al. | Apr 2008 | B2 |
7357287 | Shelton, IV et al. | Apr 2008 | B2 |
7357802 | Palanker et al. | Apr 2008 | B2 |
7361172 | Cimino | Apr 2008 | B2 |
7364577 | Wham et al. | Apr 2008 | B2 |
7367976 | Lawes et al. | May 2008 | B2 |
7371227 | Zeiner | May 2008 | B2 |
RE40388 | Gines | Jun 2008 | E |
7380695 | Doll et al. | Jun 2008 | B2 |
7380696 | Shelton, IV et al. | Jun 2008 | B2 |
7381209 | Truckai et al. | Jun 2008 | B2 |
7384420 | Dycus et al. | Jun 2008 | B2 |
7390317 | Taylor et al. | Jun 2008 | B2 |
7396356 | Mollenauer | Jul 2008 | B2 |
7403224 | Fuller et al. | Jul 2008 | B2 |
7404508 | Smith et al. | Jul 2008 | B2 |
7407077 | Ortiz et al. | Aug 2008 | B2 |
7408288 | Hara | Aug 2008 | B2 |
7412008 | Lliev | Aug 2008 | B2 |
7416101 | Shelton, IV et al. | Aug 2008 | B2 |
7416437 | Sartor et al. | Aug 2008 | B2 |
D576725 | Shumer et al. | Sep 2008 | S |
7419490 | Falkenstein et al. | Sep 2008 | B2 |
7422139 | Shelton, IV et al. | Sep 2008 | B2 |
7422463 | Kuo | Sep 2008 | B2 |
7422582 | Malackowski et al. | Sep 2008 | B2 |
D578643 | Shumer et al. | Oct 2008 | S |
D578644 | Shumer et al. | Oct 2008 | S |
D578645 | Shumer et al. | Oct 2008 | S |
7431704 | Babaev | Oct 2008 | B2 |
7431720 | Pendekanti et al. | Oct 2008 | B2 |
7435582 | Zimmermann et al. | Oct 2008 | B2 |
7441684 | Shelton, IV et al. | Oct 2008 | B2 |
7442193 | Shields et al. | Oct 2008 | B2 |
7445621 | Dumbauld et al. | Nov 2008 | B2 |
7455208 | Wales et al. | Nov 2008 | B2 |
7462181 | Kraft et al. | Dec 2008 | B2 |
7464846 | Shelton, IV et al. | Dec 2008 | B2 |
7472815 | Shelton, IV et al. | Jan 2009 | B2 |
7473145 | Ehr et al. | Jan 2009 | B2 |
7473253 | Dycus et al. | Jan 2009 | B2 |
7473263 | Johnston et al. | Jan 2009 | B2 |
7479148 | Beaupre | Jan 2009 | B2 |
7479160 | Branch et al. | Jan 2009 | B2 |
7481775 | Weikel, Jr. et al. | Jan 2009 | B2 |
7488285 | Honda et al. | Feb 2009 | B2 |
7488319 | Yates | Feb 2009 | B2 |
7491201 | Shields et al. | Feb 2009 | B2 |
7494468 | Rabiner et al. | Feb 2009 | B2 |
7494501 | Ahlberg et al. | Feb 2009 | B2 |
7498080 | Tung et al. | Mar 2009 | B2 |
7502234 | Goliszek et al. | Mar 2009 | B2 |
7503893 | Kucklick | Mar 2009 | B2 |
7503895 | Rabiner et al. | Mar 2009 | B2 |
7506790 | Shelton, IV | Mar 2009 | B2 |
7506791 | Omaits et al. | Mar 2009 | B2 |
7510107 | Timm et al. | Mar 2009 | B2 |
7513025 | Fischer | Apr 2009 | B2 |
7517349 | Truckai et al. | Apr 2009 | B2 |
7524320 | Tierney et al. | Apr 2009 | B2 |
7530986 | Beaupre et al. | May 2009 | B2 |
7534243 | Chin et al. | May 2009 | B1 |
7535233 | Kojovic et al. | May 2009 | B2 |
D594983 | Price et al. | Jun 2009 | S |
7540871 | Gonnering | Jun 2009 | B2 |
7540872 | Schechter et al. | Jun 2009 | B2 |
7543730 | Marczyk | Jun 2009 | B1 |
7544200 | Houser | Jun 2009 | B2 |
7549564 | Boudreaux | Jun 2009 | B2 |
7550216 | Ofer et al. | Jun 2009 | B2 |
7553309 | Buysse et al. | Jun 2009 | B2 |
7554343 | Bromfield | Jun 2009 | B2 |
7559450 | Wales et al. | Jul 2009 | B2 |
7559452 | Wales et al. | Jul 2009 | B2 |
7566318 | Haefner | Jul 2009 | B2 |
7567012 | Namikawa | Jul 2009 | B2 |
7568603 | Shelton, IV et al. | Aug 2009 | B2 |
7569057 | Liu et al. | Aug 2009 | B2 |
7572266 | Young et al. | Aug 2009 | B2 |
7572268 | Babaev | Aug 2009 | B2 |
7578820 | Moore et al. | Aug 2009 | B2 |
7582084 | Swanson et al. | Sep 2009 | B2 |
7582086 | Privitera et al. | Sep 2009 | B2 |
7582087 | Tetzlaff et al. | Sep 2009 | B2 |
7582095 | Shipp et al. | Sep 2009 | B2 |
7585181 | Olsen | Sep 2009 | B2 |
7586289 | Andruk et al. | Sep 2009 | B2 |
7587536 | McLeod | Sep 2009 | B2 |
7588176 | Timm et al. | Sep 2009 | B2 |
7594925 | Danek et al. | Sep 2009 | B2 |
7597693 | Garrison | Oct 2009 | B2 |
7601119 | Shahinian | Oct 2009 | B2 |
7601136 | Akahoshi | Oct 2009 | B2 |
7604150 | Boudreaux | Oct 2009 | B2 |
7607557 | Shelton, IV et al. | Oct 2009 | B2 |
7621930 | Houser | Nov 2009 | B2 |
7628791 | Garrison et al. | Dec 2009 | B2 |
7628792 | Guerra | Dec 2009 | B2 |
7632267 | Dahla | Dec 2009 | B2 |
7632269 | Truckai et al. | Dec 2009 | B2 |
7641653 | Dalla Betta et al. | Jan 2010 | B2 |
7641671 | Crainich | Jan 2010 | B2 |
7644848 | Swayze et al. | Jan 2010 | B2 |
7645240 | Thompson et al. | Jan 2010 | B2 |
7645277 | McClurken et al. | Jan 2010 | B2 |
7645278 | Ichihashi et al. | Jan 2010 | B2 |
7648499 | Orszulak et al. | Jan 2010 | B2 |
7654431 | Hueil et al. | Feb 2010 | B2 |
7655003 | Lorang et al. | Feb 2010 | B2 |
7658311 | Boudreaux | Feb 2010 | B2 |
7659833 | Warner et al. | Feb 2010 | B2 |
7662151 | Crompton, Jr. et al. | Feb 2010 | B2 |
7665647 | Shelton, IV et al. | Feb 2010 | B2 |
7666206 | Taniguchi et al. | Feb 2010 | B2 |
7667592 | Ohyama et al. | Feb 2010 | B2 |
7670334 | Hueil et al. | Mar 2010 | B2 |
7670338 | Albrecht et al. | Mar 2010 | B2 |
7674263 | Ryan | Mar 2010 | B2 |
7678069 | Baker et al. | Mar 2010 | B1 |
7678105 | McGreevy et al. | Mar 2010 | B2 |
7678125 | Shipp | Mar 2010 | B2 |
7682366 | Sakurai et al. | Mar 2010 | B2 |
7686770 | Cohen | Mar 2010 | B2 |
7686826 | Lee et al. | Mar 2010 | B2 |
7688028 | Phillips et al. | Mar 2010 | B2 |
7691095 | Bednarek et al. | Apr 2010 | B2 |
7691098 | Wallace et al. | Apr 2010 | B2 |
7699846 | Ryan | Apr 2010 | B2 |
7703459 | Saadat et al. | Apr 2010 | B2 |
7703653 | Shah et al. | Apr 2010 | B2 |
7708735 | Chapman et al. | May 2010 | B2 |
7708751 | Hughes et al. | May 2010 | B2 |
7708768 | Danek et al. | May 2010 | B2 |
7713202 | Boukhny et al. | May 2010 | B2 |
7714481 | Sakai | May 2010 | B2 |
7717312 | Beetel | May 2010 | B2 |
7717915 | Miyazawa | May 2010 | B2 |
7721935 | Racenet et al. | May 2010 | B2 |
7722527 | Bouchier et al. | May 2010 | B2 |
7722607 | Dumbauld et al. | May 2010 | B2 |
D618797 | Price et al. | Jun 2010 | S |
7726537 | Olson et al. | Jun 2010 | B2 |
7727177 | Bayat | Jun 2010 | B2 |
7738969 | Bleich | Jun 2010 | B2 |
7740594 | Hibner | Jun 2010 | B2 |
7744615 | Couture | Jun 2010 | B2 |
7751115 | Song | Jul 2010 | B2 |
7753904 | Shelton, IV et al. | Jul 2010 | B2 |
7753908 | Swanson | Jul 2010 | B2 |
7762445 | Heinrich et al. | Jul 2010 | B2 |
D621503 | Otten et al. | Aug 2010 | S |
7766210 | Shelton, IV et al. | Aug 2010 | B2 |
7766693 | Sartor et al. | Aug 2010 | B2 |
7766910 | Hixson et al. | Aug 2010 | B2 |
7768510 | Tsai et al. | Aug 2010 | B2 |
7770774 | Mastri et al. | Aug 2010 | B2 |
7770775 | Shelton, IV et al. | Aug 2010 | B2 |
7771425 | Dycus et al. | Aug 2010 | B2 |
7771444 | Patel et al. | Aug 2010 | B2 |
7775972 | Brock et al. | Aug 2010 | B2 |
7776036 | Schechter et al. | Aug 2010 | B2 |
7776037 | Odom | Aug 2010 | B2 |
7778733 | Nowlin et al. | Aug 2010 | B2 |
7780054 | Wales | Aug 2010 | B2 |
7780593 | Ueno et al. | Aug 2010 | B2 |
7780651 | Madhani et al. | Aug 2010 | B2 |
7780659 | Okada et al. | Aug 2010 | B2 |
7780663 | Yates et al. | Aug 2010 | B2 |
7784662 | Wales et al. | Aug 2010 | B2 |
7784663 | Shelton, IV | Aug 2010 | B2 |
7789883 | Takashino et al. | Sep 2010 | B2 |
7793814 | Racenet et al. | Sep 2010 | B2 |
7796969 | Kelly et al. | Sep 2010 | B2 |
7798386 | Schall et al. | Sep 2010 | B2 |
7799020 | Shores et al. | Sep 2010 | B2 |
7799027 | Hafner | Sep 2010 | B2 |
7799045 | Masuda | Sep 2010 | B2 |
7803152 | Honda et al. | Sep 2010 | B2 |
7803156 | Eder et al. | Sep 2010 | B2 |
7806891 | Nowlin et al. | Oct 2010 | B2 |
7810693 | Broehl et al. | Oct 2010 | B2 |
7811283 | Moses et al. | Oct 2010 | B2 |
7815641 | Dodde et al. | Oct 2010 | B2 |
7819298 | Hall et al. | Oct 2010 | B2 |
7819299 | Shelton, IV et al. | Oct 2010 | B2 |
7819819 | Quick et al. | Oct 2010 | B2 |
7819872 | Johnson et al. | Oct 2010 | B2 |
7821143 | Wiener | Oct 2010 | B2 |
D627066 | Romero | Nov 2010 | S |
7824401 | Manzo et al. | Nov 2010 | B2 |
7832408 | Shelton, IV et al. | Nov 2010 | B2 |
7832611 | Boyden et al. | Nov 2010 | B2 |
7832612 | Baxter, III et al. | Nov 2010 | B2 |
7834484 | Sartor | Nov 2010 | B2 |
7837699 | Yamada et al. | Nov 2010 | B2 |
7845537 | Shelton, IV et al. | Dec 2010 | B2 |
7846155 | Houser et al. | Dec 2010 | B2 |
7846159 | Morrison et al. | Dec 2010 | B2 |
7846160 | Payne et al. | Dec 2010 | B2 |
7846161 | Dumbauld et al. | Dec 2010 | B2 |
7854735 | Houser et al. | Dec 2010 | B2 |
D631155 | Peine et al. | Jan 2011 | S |
7861906 | Doll et al. | Jan 2011 | B2 |
7862560 | Marion | Jan 2011 | B2 |
7862561 | Swanson et al. | Jan 2011 | B2 |
7871392 | Sartor | Jan 2011 | B2 |
7876030 | Taki et al. | Jan 2011 | B2 |
D631965 | Price et al. | Feb 2011 | S |
7877852 | Unger et al. | Feb 2011 | B2 |
7878991 | Babaev | Feb 2011 | B2 |
7879033 | Sartor et al. | Feb 2011 | B2 |
7879035 | Garrison et al. | Feb 2011 | B2 |
7879070 | Ortiz et al. | Feb 2011 | B2 |
7892606 | Thies et al. | Feb 2011 | B2 |
7896875 | Heim et al. | Mar 2011 | B2 |
7897792 | Iikura et al. | Mar 2011 | B2 |
7901400 | Wham et al. | Mar 2011 | B2 |
7901423 | Stulen et al. | Mar 2011 | B2 |
7905881 | Masuda et al. | Mar 2011 | B2 |
7909220 | Viola | Mar 2011 | B2 |
7909820 | Lipson et al. | Mar 2011 | B2 |
7909824 | Masuda et al. | Mar 2011 | B2 |
7918848 | Lau et al. | Apr 2011 | B2 |
7919184 | Mohapatra et al. | Apr 2011 | B2 |
7922061 | Shelton, IV et al. | Apr 2011 | B2 |
7922651 | Yamada et al. | Apr 2011 | B2 |
7931649 | Couture et al. | Apr 2011 | B2 |
D637288 | Houghton | May 2011 | S |
D638540 | Ijiri et al. | May 2011 | S |
7935114 | Takashino et al. | May 2011 | B2 |
7936203 | Zimlich | May 2011 | B2 |
7951095 | Makin et al. | May 2011 | B2 |
7951165 | Golden et al. | May 2011 | B2 |
7955331 | Truckai et al. | Jun 2011 | B2 |
7956620 | Gilbert | Jun 2011 | B2 |
7959050 | Smith et al. | Jun 2011 | B2 |
7959626 | Hong et al. | Jun 2011 | B2 |
7963963 | Francischelli et al. | Jun 2011 | B2 |
7967602 | Lindquist | Jun 2011 | B2 |
7972328 | Wham et al. | Jul 2011 | B2 |
7972329 | Refior et al. | Jul 2011 | B2 |
7976544 | McClurken et al. | Jul 2011 | B2 |
7980443 | Scheib et al. | Jul 2011 | B2 |
7981050 | Ritchart et al. | Jul 2011 | B2 |
7981113 | Truckai et al. | Jul 2011 | B2 |
7997278 | Utley et al. | Aug 2011 | B2 |
7998157 | Culp et al. | Aug 2011 | B2 |
8002770 | Swanson et al. | Aug 2011 | B2 |
8020743 | Shelton, IV | Sep 2011 | B2 |
8028885 | Smith et al. | Oct 2011 | B2 |
8033173 | Ehlert et al. | Oct 2011 | B2 |
8038693 | Allen | Oct 2011 | B2 |
8048070 | O'Brien et al. | Nov 2011 | B2 |
8052672 | Laufer et al. | Nov 2011 | B2 |
8055208 | Lilla et al. | Nov 2011 | B2 |
8056720 | Hawkes | Nov 2011 | B2 |
8056787 | Boudreaux et al. | Nov 2011 | B2 |
8057468 | Konesky | Nov 2011 | B2 |
8057498 | Robertson | Nov 2011 | B2 |
8058771 | Giordano et al. | Nov 2011 | B2 |
8061014 | Smith et al. | Nov 2011 | B2 |
8066167 | Measamer et al. | Nov 2011 | B2 |
8070036 | Knodel | Dec 2011 | B1 |
8070711 | Bassinger et al. | Dec 2011 | B2 |
8070762 | Escudero et al. | Dec 2011 | B2 |
8075555 | Truckai et al. | Dec 2011 | B2 |
8075558 | Truckai et al. | Dec 2011 | B2 |
8089197 | Rinner et al. | Jan 2012 | B2 |
8092475 | Cotter et al. | Jan 2012 | B2 |
8096459 | Ortiz et al. | Jan 2012 | B2 |
8097012 | Kagarise | Jan 2012 | B2 |
8100894 | Mucko et al. | Jan 2012 | B2 |
8105323 | Buysse et al. | Jan 2012 | B2 |
8114104 | Young et al. | Feb 2012 | B2 |
8118276 | Sanders et al. | Feb 2012 | B2 |
8128624 | Couture et al. | Mar 2012 | B2 |
8133218 | Daw et al. | Mar 2012 | B2 |
8136712 | Zingman | Mar 2012 | B2 |
8141762 | Bedi et al. | Mar 2012 | B2 |
8142421 | Cooper et al. | Mar 2012 | B2 |
8142461 | Houser et al. | Mar 2012 | B2 |
8147485 | Wham et al. | Apr 2012 | B2 |
8147508 | Madan et al. | Apr 2012 | B2 |
8152801 | Goldberg et al. | Apr 2012 | B2 |
8152825 | Madan et al. | Apr 2012 | B2 |
8157145 | Shelton, IV et al. | Apr 2012 | B2 |
8161977 | Shelton, IV et al. | Apr 2012 | B2 |
8162966 | Connor et al. | Apr 2012 | B2 |
8172846 | Brunnett et al. | May 2012 | B2 |
8172870 | Shipp | May 2012 | B2 |
8177800 | Spitz et al. | May 2012 | B2 |
8182502 | Stulen et al. | May 2012 | B2 |
8186560 | Hess et al. | May 2012 | B2 |
8186877 | Klimovitch et al. | May 2012 | B2 |
8187267 | Pappone et al. | May 2012 | B2 |
D661801 | Price et al. | Jun 2012 | S |
D661802 | Price et al. | Jun 2012 | S |
D661803 | Price et al. | Jun 2012 | S |
D661804 | Price et al. | Jun 2012 | S |
8197472 | Lau et al. | Jun 2012 | B2 |
8197479 | Olson et al. | Jun 2012 | B2 |
8197502 | Smith et al. | Jun 2012 | B2 |
8207651 | Gilbert | Jun 2012 | B2 |
8210411 | Yates et al. | Jul 2012 | B2 |
8211100 | Podhajsky et al. | Jul 2012 | B2 |
8221415 | Francischelli | Jul 2012 | B2 |
8226580 | Govari et al. | Jul 2012 | B2 |
8226675 | Houser et al. | Jul 2012 | B2 |
8231607 | Takuma | Jul 2012 | B2 |
8235917 | Joseph et al. | Aug 2012 | B2 |
8236018 | Yoshimine et al. | Aug 2012 | B2 |
8236019 | Houser | Aug 2012 | B2 |
8236020 | Smith et al. | Aug 2012 | B2 |
8241235 | Kahler et al. | Aug 2012 | B2 |
8241271 | Millman et al. | Aug 2012 | B2 |
8241282 | Unger et al. | Aug 2012 | B2 |
8241283 | Guerra et al. | Aug 2012 | B2 |
8241284 | Dycus et al. | Aug 2012 | B2 |
8241312 | Messerly | Aug 2012 | B2 |
8246575 | Viola | Aug 2012 | B2 |
8246615 | Behnke | Aug 2012 | B2 |
8246616 | Amoah et al. | Aug 2012 | B2 |
8246618 | Bucciaglia et al. | Aug 2012 | B2 |
8251994 | McKenna et al. | Aug 2012 | B2 |
8252012 | Stulen | Aug 2012 | B2 |
8253303 | Giordano et al. | Aug 2012 | B2 |
8257377 | Wiener et al. | Sep 2012 | B2 |
8257387 | Cunningham | Sep 2012 | B2 |
8262563 | Bakos et al. | Sep 2012 | B2 |
8267300 | Boudreaux | Sep 2012 | B2 |
8267935 | Couture et al. | Sep 2012 | B2 |
8273087 | Kimura et al. | Sep 2012 | B2 |
D669992 | Schafer et al. | Oct 2012 | S |
D669993 | Merchant et al. | Oct 2012 | S |
8277446 | Heard | Oct 2012 | B2 |
8277447 | Garrison et al. | Oct 2012 | B2 |
8277471 | Wiener et al. | Oct 2012 | B2 |
8282669 | Gerber et al. | Oct 2012 | B2 |
8286846 | Smith et al. | Oct 2012 | B2 |
8287485 | Kimura et al. | Oct 2012 | B2 |
8287528 | Wham et al. | Oct 2012 | B2 |
8287532 | Carroll et al. | Oct 2012 | B2 |
8292886 | Kerr et al. | Oct 2012 | B2 |
8292888 | Whitman | Oct 2012 | B2 |
8292905 | Taylor et al. | Oct 2012 | B2 |
8295902 | Salahieh et al. | Oct 2012 | B2 |
8298223 | Wham et al. | Oct 2012 | B2 |
8298225 | Gilbert | Oct 2012 | B2 |
8298232 | Unger | Oct 2012 | B2 |
8298233 | Mueller | Oct 2012 | B2 |
8303576 | Brock | Nov 2012 | B2 |
8303579 | Shibata | Nov 2012 | B2 |
8303580 | Wham et al. | Nov 2012 | B2 |
8303583 | Hosier et al. | Nov 2012 | B2 |
8303613 | Crandall et al. | Nov 2012 | B2 |
8306629 | Mioduski et al. | Nov 2012 | B2 |
8308040 | Huang et al. | Nov 2012 | B2 |
8319400 | Houser et al. | Nov 2012 | B2 |
8323302 | Robertson et al. | Dec 2012 | B2 |
8323310 | Kingsley | Dec 2012 | B2 |
8328761 | Widenhouse et al. | Dec 2012 | B2 |
8328802 | Deville et al. | Dec 2012 | B2 |
8328833 | Cuny | Dec 2012 | B2 |
8328834 | Isaacs et al. | Dec 2012 | B2 |
8333778 | Smith et al. | Dec 2012 | B2 |
8333779 | Smith et al. | Dec 2012 | B2 |
8334468 | Palmer et al. | Dec 2012 | B2 |
8334635 | Voegele et al. | Dec 2012 | B2 |
8337407 | Quistgaard et al. | Dec 2012 | B2 |
8338726 | Palmer et al. | Dec 2012 | B2 |
8344596 | Nield et al. | Jan 2013 | B2 |
8348880 | Messerly et al. | Jan 2013 | B2 |
8348947 | Takashino et al. | Jan 2013 | B2 |
8348967 | Stulen | Jan 2013 | B2 |
8357103 | Mark et al. | Jan 2013 | B2 |
8357149 | Govari et al. | Jan 2013 | B2 |
8357158 | McKenna et al. | Jan 2013 | B2 |
8361066 | Long et al. | Jan 2013 | B2 |
8361072 | Dumbauld et al. | Jan 2013 | B2 |
8361569 | Saito et al. | Jan 2013 | B2 |
8366727 | Witt et al. | Feb 2013 | B2 |
8372064 | Douglass et al. | Feb 2013 | B2 |
8372099 | Deville et al. | Feb 2013 | B2 |
8372101 | Smith et al. | Feb 2013 | B2 |
8372102 | Stulen et al. | Feb 2013 | B2 |
8374670 | Selkee | Feb 2013 | B2 |
8377044 | Coe et al. | Feb 2013 | B2 |
8377059 | Deville et al. | Feb 2013 | B2 |
8377085 | Smith et al. | Feb 2013 | B2 |
8382748 | Geisel | Feb 2013 | B2 |
8382775 | Bender et al. | Feb 2013 | B1 |
8382782 | Robertson et al. | Feb 2013 | B2 |
8382792 | Chojin | Feb 2013 | B2 |
8397971 | Yates et al. | Mar 2013 | B2 |
8403945 | Whitfield et al. | Mar 2013 | B2 |
8403948 | Deville et al. | Mar 2013 | B2 |
8403949 | Palmer et al. | Mar 2013 | B2 |
8403950 | Palmer et al. | Mar 2013 | B2 |
8409234 | Stahler et al. | Apr 2013 | B2 |
8414577 | Boudreaux et al. | Apr 2013 | B2 |
8418073 | Mohr et al. | Apr 2013 | B2 |
8418349 | Smith et al. | Apr 2013 | B2 |
8419757 | Smith et al. | Apr 2013 | B2 |
8419758 | Smith et al. | Apr 2013 | B2 |
8419759 | Dietz | Apr 2013 | B2 |
8423182 | Robinson et al. | Apr 2013 | B2 |
8425410 | Murray et al. | Apr 2013 | B2 |
8425545 | Smith et al. | Apr 2013 | B2 |
8430811 | Hess et al. | Apr 2013 | B2 |
8430876 | Kappus et al. | Apr 2013 | B2 |
8430897 | Novak et al. | Apr 2013 | B2 |
8430898 | Wiener et al. | Apr 2013 | B2 |
8435257 | Smith et al. | May 2013 | B2 |
8439912 | Cunningham et al. | May 2013 | B2 |
8439939 | Deville et al. | May 2013 | B2 |
8444637 | Podmore et al. | May 2013 | B2 |
8444662 | Palmer et al. | May 2013 | B2 |
8444664 | Balanev et al. | May 2013 | B2 |
8453906 | Huang et al. | Jun 2013 | B2 |
8454639 | Du et al. | Jun 2013 | B2 |
8459525 | Yates et al. | Jun 2013 | B2 |
8460284 | Aronow et al. | Jun 2013 | B2 |
8460288 | Tamai et al. | Jun 2013 | B2 |
8460292 | Truckai et al. | Jun 2013 | B2 |
8461744 | Wiener et al. | Jun 2013 | B2 |
8469981 | Robertson et al. | Jun 2013 | B2 |
8479969 | Shelton, IV | Jul 2013 | B2 |
8480703 | Nicholas et al. | Jul 2013 | B2 |
8484833 | Cunningham et al. | Jul 2013 | B2 |
8485413 | Scheib et al. | Jul 2013 | B2 |
8485970 | Widenhouse et al. | Jul 2013 | B2 |
8486057 | Behnke, II | Jul 2013 | B2 |
8486096 | Robertson et al. | Jul 2013 | B2 |
8491578 | Manwaring et al. | Jul 2013 | B2 |
8491625 | Horner | Jul 2013 | B2 |
8496682 | Guerra et al. | Jul 2013 | B2 |
D687549 | Johnson et al. | Aug 2013 | S |
8506555 | Ruiz Morales | Aug 2013 | B2 |
8509318 | Tailliet | Aug 2013 | B2 |
8512336 | Couture | Aug 2013 | B2 |
8512337 | Francischelli et al. | Aug 2013 | B2 |
8512359 | Whitman et al. | Aug 2013 | B2 |
8512364 | Kowalski et al. | Aug 2013 | B2 |
8512365 | Wiener et al. | Aug 2013 | B2 |
8518067 | Masuda et al. | Aug 2013 | B2 |
8521331 | Itkowitz | Aug 2013 | B2 |
8523882 | Huitema et al. | Sep 2013 | B2 |
8523889 | Stulen et al. | Sep 2013 | B2 |
8528563 | Gruber | Sep 2013 | B2 |
8529437 | Taylor et al. | Sep 2013 | B2 |
8529565 | Masuda et al. | Sep 2013 | B2 |
8531064 | Robertson et al. | Sep 2013 | B2 |
8535311 | Schall | Sep 2013 | B2 |
8535340 | Allen | Sep 2013 | B2 |
8535341 | Allen | Sep 2013 | B2 |
8540128 | Shelton, IV et al. | Sep 2013 | B2 |
8546996 | Messerly et al. | Oct 2013 | B2 |
8546999 | Houser et al. | Oct 2013 | B2 |
8551077 | Main et al. | Oct 2013 | B2 |
8551086 | Kimura et al. | Oct 2013 | B2 |
8562592 | Conlon et al. | Oct 2013 | B2 |
8562598 | Falkenstein et al. | Oct 2013 | B2 |
8562600 | Kirkpatrick et al. | Oct 2013 | B2 |
8562604 | Nishimura | Oct 2013 | B2 |
8568390 | Mueller | Oct 2013 | B2 |
8568397 | Horner et al. | Oct 2013 | B2 |
8568400 | Gilbert | Oct 2013 | B2 |
8568412 | Brandt et al. | Oct 2013 | B2 |
8569997 | Lee | Oct 2013 | B2 |
8573461 | Shelton, IV et al. | Nov 2013 | B2 |
8573465 | Shelton, IV | Nov 2013 | B2 |
8574231 | Boudreaux et al. | Nov 2013 | B2 |
8574253 | Gruber et al. | Nov 2013 | B2 |
8579176 | Smith et al. | Nov 2013 | B2 |
8579897 | Vakharia et al. | Nov 2013 | B2 |
8579928 | Robertson et al. | Nov 2013 | B2 |
8585727 | Polo | Nov 2013 | B2 |
8588371 | Ogawa et al. | Nov 2013 | B2 |
8591459 | Clymer et al. | Nov 2013 | B2 |
8591506 | Wham et al. | Nov 2013 | B2 |
8591536 | Robertson | Nov 2013 | B2 |
D695407 | Price et al. | Dec 2013 | S |
D696631 | Price et al. | Dec 2013 | S |
8597193 | Grunwald et al. | Dec 2013 | B2 |
8602031 | Reis et al. | Dec 2013 | B2 |
8602288 | Shelton, IV et al. | Dec 2013 | B2 |
8603089 | Viola | Dec 2013 | B2 |
8608044 | Hueil et al. | Dec 2013 | B2 |
8608745 | Guzman et al. | Dec 2013 | B2 |
8613383 | Beckman et al. | Dec 2013 | B2 |
8616431 | Timm et al. | Dec 2013 | B2 |
8617194 | Beaupre | Dec 2013 | B2 |
8622274 | Yates et al. | Jan 2014 | B2 |
8623011 | Spivey | Jan 2014 | B2 |
8623016 | Fischer | Jan 2014 | B2 |
8623027 | Price et al. | Jan 2014 | B2 |
8623044 | Timm et al. | Jan 2014 | B2 |
8628529 | Aldridge et al. | Jan 2014 | B2 |
8632461 | Glossop | Jan 2014 | B2 |
8638428 | Brown | Jan 2014 | B2 |
8640788 | Dachs, II et al. | Feb 2014 | B2 |
8647350 | Mohan et al. | Feb 2014 | B2 |
8650728 | Wan et al. | Feb 2014 | B2 |
8652120 | Giordano et al. | Feb 2014 | B2 |
8652132 | Tsuchiya et al. | Feb 2014 | B2 |
8652155 | Houser et al. | Feb 2014 | B2 |
8657489 | Ladurner et al. | Feb 2014 | B2 |
8659208 | Rose et al. | Feb 2014 | B1 |
8663220 | Wiener et al. | Mar 2014 | B2 |
8663222 | Anderson et al. | Mar 2014 | B2 |
8663223 | Masuda et al. | Mar 2014 | B2 |
8663262 | Smith et al. | Mar 2014 | B2 |
8668691 | Heard | Mar 2014 | B2 |
8668710 | Slipszenko et al. | Mar 2014 | B2 |
8684253 | Giordano et al. | Apr 2014 | B2 |
8685016 | Wham et al. | Apr 2014 | B2 |
8685020 | Weizman et al. | Apr 2014 | B2 |
8690582 | Rohrbach et al. | Apr 2014 | B2 |
8696366 | Chen et al. | Apr 2014 | B2 |
8696665 | Hunt et al. | Apr 2014 | B2 |
8696666 | Sanai et al. | Apr 2014 | B2 |
8702609 | Hadjicostis | Apr 2014 | B2 |
8702704 | Shelton, IV et al. | Apr 2014 | B2 |
8704425 | Giordano et al. | Apr 2014 | B2 |
8708213 | Shelton, IV et al. | Apr 2014 | B2 |
8709031 | Stulen | Apr 2014 | B2 |
8709035 | Johnson et al. | Apr 2014 | B2 |
8715270 | Weitzner et al. | May 2014 | B2 |
8715277 | Weizman | May 2014 | B2 |
8721640 | Taylor et al. | May 2014 | B2 |
8721657 | Kondoh et al. | May 2014 | B2 |
8734443 | Hixson et al. | May 2014 | B2 |
8747238 | Shelton, IV et al. | Jun 2014 | B2 |
8747351 | Schultz | Jun 2014 | B2 |
8747404 | Boudreaux et al. | Jun 2014 | B2 |
8749116 | Messerly et al. | Jun 2014 | B2 |
8752264 | Ackley et al. | Jun 2014 | B2 |
8752749 | Moore et al. | Jun 2014 | B2 |
8753338 | Widenhouse et al. | Jun 2014 | B2 |
8754570 | Voegele et al. | Jun 2014 | B2 |
8758342 | Bales et al. | Jun 2014 | B2 |
8758352 | Cooper et al. | Jun 2014 | B2 |
8764735 | Coe et al. | Jul 2014 | B2 |
8764747 | Cummings et al. | Jul 2014 | B2 |
8767970 | Eppolito | Jul 2014 | B2 |
8770459 | Racenet et al. | Jul 2014 | B2 |
8771269 | Sherman et al. | Jul 2014 | B2 |
8771270 | Burbank | Jul 2014 | B2 |
8771293 | Surti et al. | Jul 2014 | B2 |
8773001 | Wiener et al. | Jul 2014 | B2 |
8777944 | Frankhouser et al. | Jul 2014 | B2 |
8779648 | Giordano et al. | Jul 2014 | B2 |
8783541 | Shelton, IV et al. | Jul 2014 | B2 |
8784415 | Malackowski et al. | Jul 2014 | B2 |
8784418 | Romero | Jul 2014 | B2 |
8790342 | Stulen et al. | Jul 2014 | B2 |
8795274 | Hanna | Aug 2014 | B2 |
8795276 | Dietz et al. | Aug 2014 | B2 |
8795327 | Dietz et al. | Aug 2014 | B2 |
8800838 | Shelton, IV | Aug 2014 | B2 |
8801710 | Ullrich et al. | Aug 2014 | B2 |
8808204 | Irisawa et al. | Aug 2014 | B2 |
8808319 | Houser et al. | Aug 2014 | B2 |
8814856 | Elmouelhi et al. | Aug 2014 | B2 |
8814870 | Paraschiv et al. | Aug 2014 | B2 |
8820605 | Shelton, IV | Sep 2014 | B2 |
8821388 | Naito et al. | Sep 2014 | B2 |
8827992 | Koss et al. | Sep 2014 | B2 |
8834466 | Cummings et al. | Sep 2014 | B2 |
8834518 | Faller et al. | Sep 2014 | B2 |
8844789 | Shelton, IV et al. | Sep 2014 | B2 |
8845537 | Tanaka et al. | Sep 2014 | B2 |
8845630 | Mehta et al. | Sep 2014 | B2 |
8848808 | Dress | Sep 2014 | B2 |
8851354 | Swensgard et al. | Oct 2014 | B2 |
8852184 | Kucklick | Oct 2014 | B2 |
8858547 | Brogna | Oct 2014 | B2 |
8862955 | Cesari | Oct 2014 | B2 |
8864749 | Okada | Oct 2014 | B2 |
8864757 | Klimovitch et al. | Oct 2014 | B2 |
8864761 | Johnson et al. | Oct 2014 | B2 |
8870865 | Frankhouser et al. | Oct 2014 | B2 |
8876726 | Amit et al. | Nov 2014 | B2 |
8876858 | Braun | Nov 2014 | B2 |
8882766 | Couture et al. | Nov 2014 | B2 |
8882791 | Stulen | Nov 2014 | B2 |
8888776 | Dietz et al. | Nov 2014 | B2 |
8888783 | Young | Nov 2014 | B2 |
8888809 | Davison et al. | Nov 2014 | B2 |
8899462 | Kostrzewski et al. | Dec 2014 | B2 |
8900259 | Houser et al. | Dec 2014 | B2 |
8906016 | Boudreaux et al. | Dec 2014 | B2 |
8906017 | Rioux et al. | Dec 2014 | B2 |
8911438 | Swoyer et al. | Dec 2014 | B2 |
8911460 | Neurohr et al. | Dec 2014 | B2 |
8920412 | Fritz et al. | Dec 2014 | B2 |
8920421 | Rupp | Dec 2014 | B2 |
8926607 | Norvell et al. | Jan 2015 | B2 |
8926608 | Bacher et al. | Jan 2015 | B2 |
8926620 | Chasmawala et al. | Jan 2015 | B2 |
8931682 | Timm et al. | Jan 2015 | B2 |
8932282 | Gilbert | Jan 2015 | B2 |
8932299 | Bono et al. | Jan 2015 | B2 |
8936614 | Allen, IV | Jan 2015 | B2 |
8939974 | Boudreaux et al. | Jan 2015 | B2 |
8951248 | Messerly et al. | Feb 2015 | B2 |
8951272 | Robertson et al. | Feb 2015 | B2 |
8956349 | Aldridge et al. | Feb 2015 | B2 |
8960520 | McCuen | Feb 2015 | B2 |
8961515 | Twomey et al. | Feb 2015 | B2 |
8961547 | Dietz et al. | Feb 2015 | B2 |
8967443 | McCuen | Mar 2015 | B2 |
8968283 | Kharin | Mar 2015 | B2 |
8968294 | Maass et al. | Mar 2015 | B2 |
8968355 | Malkowski et al. | Mar 2015 | B2 |
8974447 | Kimball et al. | Mar 2015 | B2 |
8974477 | Yamada | Mar 2015 | B2 |
8974479 | Ross et al. | Mar 2015 | B2 |
8979843 | Timm et al. | Mar 2015 | B2 |
8979844 | White et al. | Mar 2015 | B2 |
8979890 | Boudreaux | Mar 2015 | B2 |
8986287 | Park et al. | Mar 2015 | B2 |
8986297 | Daniel et al. | Mar 2015 | B2 |
8986302 | Aldridge et al. | Mar 2015 | B2 |
8989903 | Weir et al. | Mar 2015 | B2 |
8991678 | Wellman et al. | Mar 2015 | B2 |
8992422 | Spivey et al. | Mar 2015 | B2 |
9005199 | Beckman et al. | Apr 2015 | B2 |
9011437 | Woodruff et al. | Apr 2015 | B2 |
9011471 | Timm et al. | Apr 2015 | B2 |
9017326 | DiNardo et al. | Apr 2015 | B2 |
9017355 | Smith et al. | Apr 2015 | B2 |
9023071 | Miller et al. | May 2015 | B2 |
9028397 | Naito | May 2015 | B2 |
9028476 | Bonn | May 2015 | B2 |
9028478 | Mueller | May 2015 | B2 |
9028494 | Shelton, IV et al. | May 2015 | B2 |
9028519 | Yates et al. | May 2015 | B2 |
9031667 | Williams | May 2015 | B2 |
9033973 | Krapohl et al. | May 2015 | B2 |
9035741 | Hamel et al. | May 2015 | B2 |
9037259 | Mathur | May 2015 | B2 |
9039690 | Kersten | May 2015 | B2 |
9039695 | Giordano et al. | May 2015 | B2 |
9039731 | Joseph | May 2015 | B2 |
9043018 | Mohr | May 2015 | B2 |
9044227 | Shelton, IV et al. | Jun 2015 | B2 |
9044238 | Orszulak | Jun 2015 | B2 |
9044243 | Johnson et al. | Jun 2015 | B2 |
9044245 | Condie et al. | Jun 2015 | B2 |
9044256 | Cadeddu et al. | Jun 2015 | B2 |
9044261 | Houser | Jun 2015 | B2 |
9050093 | Aldridge et al. | Jun 2015 | B2 |
9050098 | Deville et al. | Jun 2015 | B2 |
9050123 | Krause et al. | Jun 2015 | B2 |
9050124 | Houser | Jun 2015 | B2 |
9055961 | Manzo et al. | Jun 2015 | B2 |
9059547 | McLawhorn | Jun 2015 | B2 |
9060770 | Shelton, IV et al. | Jun 2015 | B2 |
9060775 | Wiener et al. | Jun 2015 | B2 |
9060776 | Yates et al. | Jun 2015 | B2 |
9066720 | Ballakur et al. | Jun 2015 | B2 |
9066723 | Beller et al. | Jun 2015 | B2 |
9066747 | Robertson | Jun 2015 | B2 |
9072523 | Houser et al. | Jul 2015 | B2 |
9072535 | Shelton, IV et al. | Jul 2015 | B2 |
9072536 | Shelton, IV et al. | Jul 2015 | B2 |
9072539 | Messerly et al. | Jul 2015 | B2 |
9084624 | Larkin et al. | Jul 2015 | B2 |
9089327 | Worrell et al. | Jul 2015 | B2 |
9089360 | Messerly et al. | Jul 2015 | B2 |
9095362 | Dachs, II et al. | Aug 2015 | B2 |
9095367 | Olson et al. | Aug 2015 | B2 |
9101385 | Shelton, IV et al. | Aug 2015 | B2 |
9107689 | Robertson et al. | Aug 2015 | B2 |
9107690 | Bales, Jr. et al. | Aug 2015 | B2 |
9113900 | Buysse et al. | Aug 2015 | B2 |
9113907 | Allen, IV et al. | Aug 2015 | B2 |
9113940 | Twomey | Aug 2015 | B2 |
9119657 | Shelton, IV et al. | Sep 2015 | B2 |
9119957 | Gantz et al. | Sep 2015 | B2 |
9125662 | Shelton, IV | Sep 2015 | B2 |
9125667 | Stone et al. | Sep 2015 | B2 |
9144453 | Rencher et al. | Sep 2015 | B2 |
9147965 | Lee | Sep 2015 | B2 |
9149324 | Huang et al. | Oct 2015 | B2 |
9149325 | Worrell et al. | Oct 2015 | B2 |
9161803 | Yates et al. | Oct 2015 | B2 |
9165114 | Jain et al. | Oct 2015 | B2 |
9168085 | Juzkiw et al. | Oct 2015 | B2 |
9168089 | Buysse et al. | Oct 2015 | B2 |
9179912 | Yates et al. | Nov 2015 | B2 |
9186204 | Nishimura et al. | Nov 2015 | B2 |
9186796 | Ogawa | Nov 2015 | B2 |
9192380 | Racenet et al. | Nov 2015 | B2 |
9192421 | Garrison | Nov 2015 | B2 |
9192428 | Houser et al. | Nov 2015 | B2 |
9192431 | Woodruff et al. | Nov 2015 | B2 |
9198714 | Worrell et al. | Dec 2015 | B2 |
9198776 | Young | Dec 2015 | B2 |
9204879 | Shelton, IV | Dec 2015 | B2 |
9204891 | Weitzman | Dec 2015 | B2 |
9204918 | Germain et al. | Dec 2015 | B2 |
9204923 | Manzo et al. | Dec 2015 | B2 |
9216050 | Condie et al. | Dec 2015 | B2 |
9216051 | Fischer et al. | Dec 2015 | B2 |
9216062 | Duque et al. | Dec 2015 | B2 |
9220483 | Frankhouser et al. | Dec 2015 | B2 |
9220527 | Houser et al. | Dec 2015 | B2 |
9220559 | Worrell et al. | Dec 2015 | B2 |
9226750 | Weir et al. | Jan 2016 | B2 |
9226751 | Shelton, IV et al. | Jan 2016 | B2 |
9226766 | Aldridge et al. | Jan 2016 | B2 |
9226767 | Stulen et al. | Jan 2016 | B2 |
9232979 | Parihar et al. | Jan 2016 | B2 |
9237891 | Shelton, IV | Jan 2016 | B2 |
9237921 | Messerly et al. | Jan 2016 | B2 |
9241060 | Fujisaki | Jan 2016 | B1 |
9241692 | Gunday et al. | Jan 2016 | B2 |
9241728 | Price et al. | Jan 2016 | B2 |
9241730 | Babaev | Jan 2016 | B2 |
9241731 | Boudreaux et al. | Jan 2016 | B2 |
9241768 | Sandhu et al. | Jan 2016 | B2 |
9247953 | Palmer et al. | Feb 2016 | B2 |
9254165 | Aronow et al. | Feb 2016 | B2 |
9259234 | Robertson et al. | Feb 2016 | B2 |
9259265 | Harris et al. | Feb 2016 | B2 |
9265567 | Orban, III et al. | Feb 2016 | B2 |
9265926 | Strobl et al. | Feb 2016 | B2 |
9277962 | Koss et al. | Mar 2016 | B2 |
9282974 | Shelton, IV | Mar 2016 | B2 |
9283027 | Monson et al. | Mar 2016 | B2 |
9283045 | Rhee et al. | Mar 2016 | B2 |
9289256 | Shelton, IV et al. | Mar 2016 | B2 |
9295514 | Shelton, IV et al. | Mar 2016 | B2 |
9301759 | Spivey et al. | Apr 2016 | B2 |
9305497 | Seo et al. | Apr 2016 | B2 |
9307388 | Liang et al. | Apr 2016 | B2 |
9307986 | Hall et al. | Apr 2016 | B2 |
9308009 | Madan et al. | Apr 2016 | B2 |
9308014 | Fischer | Apr 2016 | B2 |
9314261 | Bales, Jr. et al. | Apr 2016 | B2 |
9314292 | Trees et al. | Apr 2016 | B2 |
9314301 | Ben-Haim et al. | Apr 2016 | B2 |
9326754 | Polster | May 2016 | B2 |
9326787 | Sanai et al. | May 2016 | B2 |
9326788 | Batross et al. | May 2016 | B2 |
9333025 | Monson et al. | May 2016 | B2 |
9339289 | Robertson | May 2016 | B2 |
9339323 | Eder et al. | May 2016 | B2 |
9339326 | McCullagh et al. | May 2016 | B2 |
9345534 | Artale et al. | May 2016 | B2 |
9345900 | Wu et al. | May 2016 | B2 |
9351642 | Nadkarni et al. | May 2016 | B2 |
9351726 | Leimbach et al. | May 2016 | B2 |
9351754 | Vakharia et al. | May 2016 | B2 |
9352173 | Yamada et al. | May 2016 | B2 |
9358065 | Ladtkow et al. | Jun 2016 | B2 |
9364230 | Shelton, IV et al. | Jun 2016 | B2 |
9370400 | Parihar | Jun 2016 | B2 |
9370611 | Ross et al. | Jun 2016 | B2 |
9375230 | Ross et al. | Jun 2016 | B2 |
9375232 | Hunt et al. | Jun 2016 | B2 |
9375256 | Cunningham et al. | Jun 2016 | B2 |
9375267 | Kerr et al. | Jun 2016 | B2 |
9385831 | Marr et al. | Jul 2016 | B2 |
9386983 | Swensgard et al. | Jul 2016 | B2 |
9393037 | Olson et al. | Jul 2016 | B2 |
9398911 | Auld | Jul 2016 | B2 |
9402680 | Ginnebaugh et al. | Aug 2016 | B2 |
9402682 | Worrell et al. | Aug 2016 | B2 |
9408606 | Shelton, IV | Aug 2016 | B2 |
9408622 | Stulen et al. | Aug 2016 | B2 |
9408660 | Strobl et al. | Aug 2016 | B2 |
9414853 | Stulen et al. | Aug 2016 | B2 |
9414880 | Monson et al. | Aug 2016 | B2 |
9421060 | Monson et al. | Aug 2016 | B2 |
9427249 | Robertson et al. | Aug 2016 | B2 |
9427279 | Muniz-Medina et al. | Aug 2016 | B2 |
9439668 | Timm et al. | Sep 2016 | B2 |
9439669 | Wiener et al. | Sep 2016 | B2 |
9439671 | Akagane | Sep 2016 | B2 |
9445832 | Wiener et al. | Sep 2016 | B2 |
9451967 | Jordan et al. | Sep 2016 | B2 |
9456863 | Moua | Oct 2016 | B2 |
9456864 | Witt et al. | Oct 2016 | B2 |
9468498 | Sigmon, Jr. | Oct 2016 | B2 |
9486236 | Price et al. | Nov 2016 | B2 |
9492146 | Kostrzewski et al. | Nov 2016 | B2 |
9492224 | Boudreaux et al. | Nov 2016 | B2 |
9498245 | Voegele et al. | Nov 2016 | B2 |
9498275 | Wham et al. | Nov 2016 | B2 |
9504483 | Houser et al. | Nov 2016 | B2 |
9504520 | Worrell et al. | Nov 2016 | B2 |
9504524 | Behnke, II | Nov 2016 | B2 |
9504855 | Messerly et al. | Nov 2016 | B2 |
9510850 | Robertson et al. | Dec 2016 | B2 |
9510906 | Boudreaux et al. | Dec 2016 | B2 |
9522029 | Yates et al. | Dec 2016 | B2 |
9522032 | Behnke | Dec 2016 | B2 |
9526564 | Rusin | Dec 2016 | B2 |
9526565 | Strobl | Dec 2016 | B2 |
9545253 | Worrell et al. | Jan 2017 | B2 |
9554846 | Boudreaux | Jan 2017 | B2 |
9554854 | Yates et al. | Jan 2017 | B2 |
9560995 | Addison et al. | Feb 2017 | B2 |
9561038 | Shelton, IV et al. | Feb 2017 | B2 |
9574644 | Parihar | Feb 2017 | B2 |
9597143 | Madan et al. | Mar 2017 | B2 |
9610091 | Johnson et al. | Apr 2017 | B2 |
9610114 | Baxter, III et al. | Apr 2017 | B2 |
9615877 | Tyrrell et al. | Apr 2017 | B2 |
9623237 | Turner et al. | Apr 2017 | B2 |
9636135 | Stulen | May 2017 | B2 |
9636165 | Larson et al. | May 2017 | B2 |
9638770 | Dietz et al. | May 2017 | B2 |
9642644 | Houser et al. | May 2017 | B2 |
9642669 | Takashino et al. | May 2017 | B2 |
9643052 | Tchao et al. | May 2017 | B2 |
9649111 | Shelton, IV et al. | May 2017 | B2 |
9649126 | Robertson et al. | May 2017 | B2 |
9655670 | Larson et al. | May 2017 | B2 |
9662131 | Omori et al. | May 2017 | B2 |
9668806 | Unger et al. | Jun 2017 | B2 |
9675374 | Stulen et al. | Jun 2017 | B2 |
9675375 | Houser et al. | Jun 2017 | B2 |
9687290 | Keller | Jun 2017 | B2 |
9700309 | Jaworek et al. | Jul 2017 | B2 |
9700339 | Nield | Jul 2017 | B2 |
9700343 | Messerly et al. | Jul 2017 | B2 |
9705456 | Gilbert | Jul 2017 | B2 |
9707004 | Houser et al. | Jul 2017 | B2 |
9707027 | Ruddenklau et al. | Jul 2017 | B2 |
9707030 | Davison et al. | Jul 2017 | B2 |
9713507 | Stulen et al. | Jul 2017 | B2 |
9717548 | Couture | Aug 2017 | B2 |
9717552 | Cosman et al. | Aug 2017 | B2 |
9724118 | Schulte et al. | Aug 2017 | B2 |
9724120 | Faller et al. | Aug 2017 | B2 |
9724152 | Horlle et al. | Aug 2017 | B2 |
9737326 | Worrell et al. | Aug 2017 | B2 |
9737355 | Yates et al. | Aug 2017 | B2 |
9737358 | Beckman et al. | Aug 2017 | B2 |
9743929 | Leimbach et al. | Aug 2017 | B2 |
9743946 | Faller et al. | Aug 2017 | B2 |
9743947 | Price et al. | Aug 2017 | B2 |
9757142 | Shimizu | Sep 2017 | B2 |
9757186 | Boudreaux et al. | Sep 2017 | B2 |
9764164 | Wiener et al. | Sep 2017 | B2 |
9770285 | Zoran et al. | Sep 2017 | B2 |
9782214 | Houser et al. | Oct 2017 | B2 |
9788851 | Dannaher et al. | Oct 2017 | B2 |
9795405 | Price et al. | Oct 2017 | B2 |
9795436 | Yates et al. | Oct 2017 | B2 |
9795808 | Messerly et al. | Oct 2017 | B2 |
9801648 | Houser et al. | Oct 2017 | B2 |
9802033 | Hibner et al. | Oct 2017 | B2 |
9808308 | Faller et al. | Nov 2017 | B2 |
9814514 | Shelton, IV et al. | Nov 2017 | B2 |
9820768 | Gee et al. | Nov 2017 | B2 |
9820771 | Norton et al. | Nov 2017 | B2 |
9820806 | Lee et al. | Nov 2017 | B2 |
9839443 | Brockman et al. | Dec 2017 | B2 |
9848901 | Robertson et al. | Dec 2017 | B2 |
9848902 | Price et al. | Dec 2017 | B2 |
9848937 | Trees et al. | Dec 2017 | B2 |
9861428 | Trees et al. | Jan 2018 | B2 |
9867651 | Wham | Jan 2018 | B2 |
9867670 | Brannan et al. | Jan 2018 | B2 |
9872722 | Lech | Jan 2018 | B2 |
9872725 | Worrell et al. | Jan 2018 | B2 |
9872726 | Morisaki | Jan 2018 | B2 |
9877720 | Worrell et al. | Jan 2018 | B2 |
9877776 | Boudreaux | Jan 2018 | B2 |
9883884 | Neurohr et al. | Feb 2018 | B2 |
9888958 | Evans et al. | Feb 2018 | B2 |
9907563 | Germain et al. | Mar 2018 | B2 |
9913656 | Stulen | Mar 2018 | B2 |
9913680 | Voegele et al. | Mar 2018 | B2 |
9918730 | Trees et al. | Mar 2018 | B2 |
9925003 | Parihar et al. | Mar 2018 | B2 |
9949785 | Price et al. | Apr 2018 | B2 |
9949788 | Boudreaux | Apr 2018 | B2 |
9962182 | Dietz et al. | May 2018 | B2 |
9974539 | Yates et al. | May 2018 | B2 |
9987033 | Neurohr et al. | Jun 2018 | B2 |
10004526 | Dycus et al. | Jun 2018 | B2 |
10010339 | Witt et al. | Jul 2018 | B2 |
10010341 | Houser et al. | Jul 2018 | B2 |
10022142 | Aranyi et al. | Jul 2018 | B2 |
10022567 | Messerly et al. | Jul 2018 | B2 |
10022568 | Messerly et al. | Jul 2018 | B2 |
10028761 | Leimbach et al. | Jul 2018 | B2 |
10028786 | Mucilli et al. | Jul 2018 | B2 |
10034684 | Weisenburgh, II et al. | Jul 2018 | B2 |
10034704 | Asher et al. | Jul 2018 | B2 |
10045794 | Witt et al. | Aug 2018 | B2 |
10045810 | Schall et al. | Aug 2018 | B2 |
10045819 | Jensen et al. | Aug 2018 | B2 |
10070916 | Artale | Sep 2018 | B2 |
10080609 | Hancock et al. | Sep 2018 | B2 |
10085762 | Timm et al. | Oct 2018 | B2 |
10085792 | Johnson et al. | Oct 2018 | B2 |
10092310 | Boudreaux et al. | Oct 2018 | B2 |
10092344 | Mohr et al. | Oct 2018 | B2 |
10092348 | Boudreaux | Oct 2018 | B2 |
10111699 | Boudreaux | Oct 2018 | B2 |
10111703 | Cosman, Jr. et al. | Oct 2018 | B2 |
10117667 | Robertson et al. | Nov 2018 | B2 |
10117702 | Danziger et al. | Nov 2018 | B2 |
10130410 | Strobl et al. | Nov 2018 | B2 |
10130412 | Wham | Nov 2018 | B2 |
10154848 | Chernov et al. | Dec 2018 | B2 |
10154852 | Conlon et al. | Dec 2018 | B2 |
10159524 | Yates et al. | Dec 2018 | B2 |
10166060 | Johnson et al. | Jan 2019 | B2 |
10172669 | Felder et al. | Jan 2019 | B2 |
10179022 | Yates et al. | Jan 2019 | B2 |
10188455 | Hancock et al. | Jan 2019 | B2 |
10194972 | Yates et al. | Feb 2019 | B2 |
10194973 | Wiener et al. | Feb 2019 | B2 |
10194976 | Boudreaux | Feb 2019 | B2 |
10194977 | Yang | Feb 2019 | B2 |
10194999 | Bacher et al. | Feb 2019 | B2 |
10201365 | Boudreaux et al. | Feb 2019 | B2 |
10201382 | Wiener et al. | Feb 2019 | B2 |
10226273 | Messerly et al. | Mar 2019 | B2 |
10231747 | Stulen et al. | Mar 2019 | B2 |
10245095 | Boudreaux | Apr 2019 | B2 |
10251664 | Shelton, IV et al. | Apr 2019 | B2 |
10263171 | Wiener et al. | Apr 2019 | B2 |
10265117 | Wiener et al. | Apr 2019 | B2 |
10265118 | Gerhardt | Apr 2019 | B2 |
20010025173 | Ritchie et al. | Sep 2001 | A1 |
20010025183 | Shahidi | Sep 2001 | A1 |
20010025184 | Messerly | Sep 2001 | A1 |
20010031950 | Ryan | Oct 2001 | A1 |
20010039419 | Francischelli et al. | Nov 2001 | A1 |
20020002377 | Cimino | Jan 2002 | A1 |
20020002380 | Bishop | Jan 2002 | A1 |
20020019649 | Sikora et al. | Feb 2002 | A1 |
20020022836 | Goble et al. | Feb 2002 | A1 |
20020029036 | Goble et al. | Mar 2002 | A1 |
20020029055 | Bonutti | Mar 2002 | A1 |
20020049551 | Friedman et al. | Apr 2002 | A1 |
20020052617 | Anis et al. | May 2002 | A1 |
20020077550 | Rabiner et al. | Jun 2002 | A1 |
20020107517 | Witt et al. | Aug 2002 | A1 |
20020156466 | Sakurai et al. | Oct 2002 | A1 |
20020156493 | Houser et al. | Oct 2002 | A1 |
20030014053 | Nguyen et al. | Jan 2003 | A1 |
20030014087 | Fang et al. | Jan 2003 | A1 |
20030036705 | Hare et al. | Feb 2003 | A1 |
20030050572 | Brautigam et al. | Mar 2003 | A1 |
20030055443 | Spotnitz | Mar 2003 | A1 |
20030109875 | Tetzlaff et al. | Jun 2003 | A1 |
20030114851 | Truckai et al. | Jun 2003 | A1 |
20030130693 | Levin et al. | Jul 2003 | A1 |
20030139741 | Goble et al. | Jul 2003 | A1 |
20030144680 | Kellogg et al. | Jul 2003 | A1 |
20030158548 | Phan et al. | Aug 2003 | A1 |
20030171747 | Kanehira et al. | Sep 2003 | A1 |
20030181898 | Bowers | Sep 2003 | A1 |
20030199794 | Sakurai et al. | Oct 2003 | A1 |
20030204199 | Novak et al. | Oct 2003 | A1 |
20030212332 | Fenton et al. | Nov 2003 | A1 |
20030212363 | Shipp | Nov 2003 | A1 |
20030212392 | Fenton et al. | Nov 2003 | A1 |
20030212422 | Fenton et al. | Nov 2003 | A1 |
20030225332 | Okada et al. | Dec 2003 | A1 |
20030229344 | Dycus et al. | Dec 2003 | A1 |
20040030254 | Babaev | Feb 2004 | A1 |
20040030330 | Brassell et al. | Feb 2004 | A1 |
20040047485 | Sherrit et al. | Mar 2004 | A1 |
20040054364 | Aranyi et al. | Mar 2004 | A1 |
20040064151 | Mollenauer | Apr 2004 | A1 |
20040087943 | Dycus et al. | May 2004 | A1 |
20040092921 | Kadziauskas et al. | May 2004 | A1 |
20040092992 | Adams et al. | May 2004 | A1 |
20040097911 | Murakami et al. | May 2004 | A1 |
20040097912 | Gonnering | May 2004 | A1 |
20040097919 | Wellman et al. | May 2004 | A1 |
20040097996 | Rabiner et al. | May 2004 | A1 |
20040116952 | Sakurai et al. | Jun 2004 | A1 |
20040122423 | Dycus et al. | Jun 2004 | A1 |
20040132383 | Langford et al. | Jul 2004 | A1 |
20040138621 | Jahns et al. | Jul 2004 | A1 |
20040142667 | Lochhead et al. | Jul 2004 | A1 |
20040147934 | Kiester | Jul 2004 | A1 |
20040147945 | Fritzsch | Jul 2004 | A1 |
20040158237 | Abboud et al. | Aug 2004 | A1 |
20040167508 | Wham et al. | Aug 2004 | A1 |
20040176686 | Hare et al. | Sep 2004 | A1 |
20040176751 | Weitzner et al. | Sep 2004 | A1 |
20040193150 | Sharkey et al. | Sep 2004 | A1 |
20040193153 | Sartor et al. | Sep 2004 | A1 |
20040199193 | Hayashi et al. | Oct 2004 | A1 |
20040215132 | Yoon | Oct 2004 | A1 |
20040243147 | Lipow | Dec 2004 | A1 |
20040249374 | Tetzlaff et al. | Dec 2004 | A1 |
20040260273 | Wan | Dec 2004 | A1 |
20040260300 | Gorensek et al. | Dec 2004 | A1 |
20040267311 | Viola et al. | Dec 2004 | A1 |
20050015125 | Mioduski et al. | Jan 2005 | A1 |
20050020967 | Ono | Jan 2005 | A1 |
20050021018 | Anderson et al. | Jan 2005 | A1 |
20050021065 | Yamada et al. | Jan 2005 | A1 |
20050021078 | Vleugels et al. | Jan 2005 | A1 |
20050033278 | McClurken et al. | Feb 2005 | A1 |
20050033337 | Muir et al. | Feb 2005 | A1 |
20050070800 | Takahashi | Mar 2005 | A1 |
20050088285 | Jei | Apr 2005 | A1 |
20050090817 | Phan | Apr 2005 | A1 |
20050096683 | Ellins et al. | May 2005 | A1 |
20050099824 | Dowling et al. | May 2005 | A1 |
20050131390 | Heinrich et al. | Jun 2005 | A1 |
20050143769 | White et al. | Jun 2005 | A1 |
20050149108 | Cox | Jul 2005 | A1 |
20050165429 | Douglas et al. | Jul 2005 | A1 |
20050171522 | Christopherson | Aug 2005 | A1 |
20050177184 | Easley | Aug 2005 | A1 |
20050182339 | Lee et al. | Aug 2005 | A1 |
20050188743 | Land | Sep 2005 | A1 |
20050192610 | Houser et al. | Sep 2005 | A1 |
20050192611 | Houser | Sep 2005 | A1 |
20050222598 | Ho et al. | Oct 2005 | A1 |
20050234484 | Houser et al. | Oct 2005 | A1 |
20050249667 | Tuszynski et al. | Nov 2005 | A1 |
20050256405 | Makin et al. | Nov 2005 | A1 |
20050261588 | Makin et al. | Nov 2005 | A1 |
20050262175 | Iino et al. | Nov 2005 | A1 |
20050267464 | Truckai et al. | Dec 2005 | A1 |
20050271807 | Iljima et al. | Dec 2005 | A1 |
20050273090 | Nieman et al. | Dec 2005 | A1 |
20050288659 | Kimura et al. | Dec 2005 | A1 |
20060025757 | Heim | Feb 2006 | A1 |
20060030797 | Zhou et al. | Feb 2006 | A1 |
20060058825 | Ogura et al. | Mar 2006 | A1 |
20060063130 | Hayman et al. | Mar 2006 | A1 |
20060064086 | Odom | Mar 2006 | A1 |
20060066181 | Bromfield et al. | Mar 2006 | A1 |
20060074442 | Noriega et al. | Apr 2006 | A1 |
20060079874 | Faller et al. | Apr 2006 | A1 |
20060079879 | Faller et al. | Apr 2006 | A1 |
20060095046 | Trieu et al. | May 2006 | A1 |
20060109061 | Dobson et al. | May 2006 | A1 |
20060159731 | Shoshan | Jul 2006 | A1 |
20060190034 | Nishizawa et al. | Aug 2006 | A1 |
20060206100 | Eskridge et al. | Sep 2006 | A1 |
20060206115 | Schomer et al. | Sep 2006 | A1 |
20060211943 | Beaupre | Sep 2006 | A1 |
20060217729 | Eskridge et al. | Sep 2006 | A1 |
20060224160 | Trieu et al. | Oct 2006 | A1 |
20060247558 | Yamada | Nov 2006 | A1 |
20060253050 | Yoshimine et al. | Nov 2006 | A1 |
20060264809 | Hansmann et al. | Nov 2006 | A1 |
20060264995 | Fanton et al. | Nov 2006 | A1 |
20060265035 | Yachi et al. | Nov 2006 | A1 |
20060270916 | Skwarek et al. | Nov 2006 | A1 |
20060271030 | Francis et al. | Nov 2006 | A1 |
20060293656 | Shadduck et al. | Dec 2006 | A1 |
20070016235 | Tanaka et al. | Jan 2007 | A1 |
20070016236 | Beaupre | Jan 2007 | A1 |
20070021738 | Hasser et al. | Jan 2007 | A1 |
20070027468 | Wales et al. | Feb 2007 | A1 |
20070055228 | Berg et al. | Mar 2007 | A1 |
20070056596 | Fanney et al. | Mar 2007 | A1 |
20070060935 | Schwardt et al. | Mar 2007 | A1 |
20070063618 | Bromfield | Mar 2007 | A1 |
20070066971 | Podhajsky | Mar 2007 | A1 |
20070067123 | Jungerman | Mar 2007 | A1 |
20070073185 | Nakao | Mar 2007 | A1 |
20070073341 | Smith et al. | Mar 2007 | A1 |
20070074584 | Talarico et al. | Apr 2007 | A1 |
20070106317 | Shelton et al. | May 2007 | A1 |
20070118115 | Artale et al. | May 2007 | A1 |
20070130771 | Ehlert et al. | Jun 2007 | A1 |
20070135803 | Belson | Jun 2007 | A1 |
20070149881 | Rabin | Jun 2007 | A1 |
20070156163 | Davison et al. | Jul 2007 | A1 |
20070166663 | Telles et al. | Jul 2007 | A1 |
20070173803 | Wham et al. | Jul 2007 | A1 |
20070173813 | Odom | Jul 2007 | A1 |
20070173872 | Neuenfeldt | Jul 2007 | A1 |
20070185474 | Nahen | Aug 2007 | A1 |
20070191712 | Messerly et al. | Aug 2007 | A1 |
20070191713 | Eichmann et al. | Aug 2007 | A1 |
20070203483 | Kim et al. | Aug 2007 | A1 |
20070208336 | Kim et al. | Sep 2007 | A1 |
20070208340 | Ganz et al. | Sep 2007 | A1 |
20070219481 | Babaev | Sep 2007 | A1 |
20070232926 | Stulen et al. | Oct 2007 | A1 |
20070232928 | Wiener et al. | Oct 2007 | A1 |
20070236213 | Paden et al. | Oct 2007 | A1 |
20070239101 | Kellogg | Oct 2007 | A1 |
20070249941 | Salehi et al. | Oct 2007 | A1 |
20070260242 | Dycus et al. | Nov 2007 | A1 |
20070265560 | Soltani et al. | Nov 2007 | A1 |
20070265613 | Edelstein et al. | Nov 2007 | A1 |
20070265616 | Couture et al. | Nov 2007 | A1 |
20070265620 | Kraas et al. | Nov 2007 | A1 |
20070275348 | Lemon | Nov 2007 | A1 |
20070287933 | Phan et al. | Dec 2007 | A1 |
20070288055 | Lee | Dec 2007 | A1 |
20070299895 | Johnson | Dec 2007 | A1 |
20080005213 | Holtzman | Jan 2008 | A1 |
20080013809 | Zhu et al. | Jan 2008 | A1 |
20080015575 | Odom et al. | Jan 2008 | A1 |
20080039746 | Hissong et al. | Feb 2008 | A1 |
20080051812 | Schmitz et al. | Feb 2008 | A1 |
20080058775 | Darian et al. | Mar 2008 | A1 |
20080058845 | Shimizu et al. | Mar 2008 | A1 |
20080071269 | Hilario et al. | Mar 2008 | A1 |
20080077145 | Boyden et al. | Mar 2008 | A1 |
20080082039 | Babaev | Apr 2008 | A1 |
20080082098 | Tanaka et al. | Apr 2008 | A1 |
20080097501 | Blier | Apr 2008 | A1 |
20080114355 | Whayne et al. | May 2008 | A1 |
20080114364 | Goldin et al. | May 2008 | A1 |
20080122496 | Wagner | May 2008 | A1 |
20080125768 | Tahara et al. | May 2008 | A1 |
20080147058 | Horrell et al. | Jun 2008 | A1 |
20080147062 | Truckai et al. | Jun 2008 | A1 |
20080147092 | Rogge et al. | Jun 2008 | A1 |
20080171938 | Masuda et al. | Jul 2008 | A1 |
20080177268 | Daum et al. | Jul 2008 | A1 |
20080188755 | Hart | Aug 2008 | A1 |
20080200940 | Eichmann et al. | Aug 2008 | A1 |
20080208108 | Kimura | Aug 2008 | A1 |
20080208231 | Ota et al. | Aug 2008 | A1 |
20080214967 | Aranyi et al. | Sep 2008 | A1 |
20080234709 | Houser | Sep 2008 | A1 |
20080243162 | Shibata et al. | Oct 2008 | A1 |
20080255413 | Zemlok et al. | Oct 2008 | A1 |
20080281200 | Voic et al. | Nov 2008 | A1 |
20080281315 | Gines | Nov 2008 | A1 |
20080287944 | Pearson et al. | Nov 2008 | A1 |
20080287948 | Newton et al. | Nov 2008 | A1 |
20080294156 | Newton | Nov 2008 | A1 |
20080296346 | Shelton, IV et al. | Dec 2008 | A1 |
20080300588 | Groth et al. | Dec 2008 | A1 |
20090012516 | Curtis et al. | Jan 2009 | A1 |
20090023985 | Ewers | Jan 2009 | A1 |
20090048537 | Lydon et al. | Feb 2009 | A1 |
20090048589 | Takashino et al. | Feb 2009 | A1 |
20090054886 | Yachi et al. | Feb 2009 | A1 |
20090054889 | Newton et al. | Feb 2009 | A1 |
20090054894 | Yachi | Feb 2009 | A1 |
20090062786 | Garito | Mar 2009 | A1 |
20090076506 | Baker | Mar 2009 | A1 |
20090082716 | Akahoshi | Mar 2009 | A1 |
20090082766 | Unger et al. | Mar 2009 | A1 |
20090088785 | Masuda | Apr 2009 | A1 |
20090090763 | Zemlok et al. | Apr 2009 | A1 |
20090118751 | Wiener et al. | May 2009 | A1 |
20090143799 | Smith et al. | Jun 2009 | A1 |
20090143800 | Deville et al. | Jun 2009 | A1 |
20090163807 | Sliwa | Jun 2009 | A1 |
20090182322 | D'Amelio et al. | Jul 2009 | A1 |
20090182331 | D'Amelio et al. | Jul 2009 | A1 |
20090182332 | Long et al. | Jul 2009 | A1 |
20090216157 | Yamada | Aug 2009 | A1 |
20090223033 | Houser | Sep 2009 | A1 |
20090240244 | Malis et al. | Sep 2009 | A1 |
20090248021 | McKenna | Oct 2009 | A1 |
20090254077 | Craig | Oct 2009 | A1 |
20090254080 | Honda | Oct 2009 | A1 |
20090264909 | Beaupre | Oct 2009 | A1 |
20090270771 | Takahashi | Oct 2009 | A1 |
20090270812 | Litscher et al. | Oct 2009 | A1 |
20090270853 | Yachi et al. | Oct 2009 | A1 |
20090270891 | Beaupre | Oct 2009 | A1 |
20090270899 | Carusillo et al. | Oct 2009 | A1 |
20090287205 | Ingle | Nov 2009 | A1 |
20090299141 | Downey et al. | Dec 2009 | A1 |
20090327715 | Smith et al. | Dec 2009 | A1 |
20100004508 | Naito et al. | Jan 2010 | A1 |
20100022825 | Yoshie | Jan 2010 | A1 |
20100030233 | Whitman et al. | Feb 2010 | A1 |
20100036370 | Mirel et al. | Feb 2010 | A1 |
20100042093 | Wham et al. | Feb 2010 | A9 |
20100049180 | Wells et al. | Feb 2010 | A1 |
20100057118 | Dietz et al. | Mar 2010 | A1 |
20100063525 | Beaupre et al. | Mar 2010 | A1 |
20100063528 | Beaupre | Mar 2010 | A1 |
20100081863 | Hess et al. | Apr 2010 | A1 |
20100081864 | Hess et al. | Apr 2010 | A1 |
20100081883 | Murray et al. | Apr 2010 | A1 |
20100094323 | Isaacs et al. | Apr 2010 | A1 |
20100106173 | Yoshimine | Apr 2010 | A1 |
20100158307 | Kubota et al. | Jun 2010 | A1 |
20100168741 | Sanai et al. | Jul 2010 | A1 |
20100187283 | Crainich et al. | Jul 2010 | A1 |
20100204721 | Young et al. | Aug 2010 | A1 |
20100217258 | Floume | Aug 2010 | A1 |
20100222714 | Muir et al. | Sep 2010 | A1 |
20100222752 | Collins, Jr. et al. | Sep 2010 | A1 |
20100228250 | Brogna | Sep 2010 | A1 |
20100234906 | Koh | Sep 2010 | A1 |
20100274160 | Yachi et al. | Oct 2010 | A1 |
20100274278 | Fleenor et al. | Oct 2010 | A1 |
20100298743 | Nield et al. | Nov 2010 | A1 |
20100331742 | Masuda | Dec 2010 | A1 |
20110004233 | Muir et al. | Jan 2011 | A1 |
20110028964 | Edwards | Feb 2011 | A1 |
20110071523 | Dickhans | Mar 2011 | A1 |
20110125149 | El-Galley et al. | May 2011 | A1 |
20110125151 | Strauss et al. | May 2011 | A1 |
20110160725 | Kabaya et al. | Jun 2011 | A1 |
20110238010 | Kirschenman et al. | Sep 2011 | A1 |
20110273465 | Konishi et al. | Nov 2011 | A1 |
20110278343 | Knodel et al. | Nov 2011 | A1 |
20110279268 | Konishi et al. | Nov 2011 | A1 |
20110284014 | Cadeddu et al. | Nov 2011 | A1 |
20110290856 | Shelton, IV et al. | Dec 2011 | A1 |
20110295295 | Shelton, IV et al. | Dec 2011 | A1 |
20110306967 | Payne et al. | Dec 2011 | A1 |
20110313415 | Fernandez et al. | Dec 2011 | A1 |
20120004655 | Kim et al. | Jan 2012 | A1 |
20120016413 | Timm et al. | Jan 2012 | A1 |
20120022519 | Huang et al. | Jan 2012 | A1 |
20120022526 | Aldridge et al. | Jan 2012 | A1 |
20120022583 | Sugalski et al. | Jan 2012 | A1 |
20120059289 | Nield et al. | Mar 2012 | A1 |
20120071863 | Lee et al. | Mar 2012 | A1 |
20120078139 | Aldridge et al. | Mar 2012 | A1 |
20120078244 | Worrell et al. | Mar 2012 | A1 |
20120080344 | Shelton, IV | Apr 2012 | A1 |
20120101495 | Young et al. | Apr 2012 | A1 |
20120109186 | Parrott et al. | May 2012 | A1 |
20120116265 | Houser et al. | May 2012 | A1 |
20120116266 | Houser et al. | May 2012 | A1 |
20120116381 | Houser et al. | May 2012 | A1 |
20120143211 | Kishi | Jun 2012 | A1 |
20120150049 | Zielinski et al. | Jun 2012 | A1 |
20120150169 | Zielinksi et al. | Jun 2012 | A1 |
20120172904 | Muir et al. | Jul 2012 | A1 |
20120211542 | Racenet | Aug 2012 | A1 |
20120253328 | Cunningham et al. | Oct 2012 | A1 |
20120265196 | Turner | Oct 2012 | A1 |
20120265241 | Hart et al. | Oct 2012 | A1 |
20120296371 | Kappus et al. | Nov 2012 | A1 |
20130023925 | Mueller | Jan 2013 | A1 |
20130035685 | Fischer et al. | Feb 2013 | A1 |
20130085510 | Stefanchik et al. | Apr 2013 | A1 |
20130123776 | Monson et al. | May 2013 | A1 |
20130158659 | Bergs et al. | Jun 2013 | A1 |
20130158660 | Bergs et al. | Jun 2013 | A1 |
20130165929 | Muir et al. | Jun 2013 | A1 |
20130214025 | Zemlok et al. | Aug 2013 | A1 |
20130253256 | Griffith et al. | Sep 2013 | A1 |
20130267943 | Hancock | Oct 2013 | A1 |
20130296843 | Boudreaux et al. | Nov 2013 | A1 |
20140001231 | Shelton, IV et al. | Jan 2014 | A1 |
20140001234 | Shelton, IV et al. | Jan 2014 | A1 |
20140005640 | Shelton, IV et al. | Jan 2014 | A1 |
20140005678 | Shelton, IV et al. | Jan 2014 | A1 |
20140005702 | Timm et al. | Jan 2014 | A1 |
20140005705 | Weir et al. | Jan 2014 | A1 |
20140005718 | Shelton, IV et al. | Jan 2014 | A1 |
20140012299 | Stoddard et al. | Jan 2014 | A1 |
20140014544 | Bugnard et al. | Jan 2014 | A1 |
20140121569 | Schafer et al. | May 2014 | A1 |
20140135804 | Weisenburgh, II et al. | May 2014 | A1 |
20140194874 | Dietz et al. | Jul 2014 | A1 |
20140194875 | Reschke et al. | Jul 2014 | A1 |
20140246475 | Hall et al. | Sep 2014 | A1 |
20140263541 | Leimbach et al. | Sep 2014 | A1 |
20140276659 | Juergens et al. | Sep 2014 | A1 |
20140276754 | Gilbert et al. | Sep 2014 | A1 |
20140276797 | Batchelor et al. | Sep 2014 | A1 |
20140276806 | Heim | Sep 2014 | A1 |
20140330271 | Dietz et al. | Nov 2014 | A1 |
20150032100 | Coulson et al. | Jan 2015 | A1 |
20150032150 | Ishida et al. | Jan 2015 | A1 |
20150080876 | Worrell et al. | Mar 2015 | A1 |
20150080887 | Sobajima et al. | Mar 2015 | A1 |
20150080912 | Sapre | Mar 2015 | A1 |
20150094703 | Zikorus et al. | Apr 2015 | A1 |
20150112335 | Boudreaux et al. | Apr 2015 | A1 |
20150157356 | Gee | Jun 2015 | A1 |
20150164533 | Felder et al. | Jun 2015 | A1 |
20150164534 | Felder et al. | Jun 2015 | A1 |
20150164535 | Felder et al. | Jun 2015 | A1 |
20150164536 | Czarnecki et al. | Jun 2015 | A1 |
20150164537 | Cagle et al. | Jun 2015 | A1 |
20150164538 | Aldridge et al. | Jun 2015 | A1 |
20150230861 | Woloszko et al. | Aug 2015 | A1 |
20150238260 | Nau, Jr. | Aug 2015 | A1 |
20150257780 | Houser | Sep 2015 | A1 |
20150272659 | Boudreaux et al. | Oct 2015 | A1 |
20150272660 | Boudreaux et al. | Oct 2015 | A1 |
20150313667 | Allen, IV | Nov 2015 | A1 |
20150320480 | Cosman, Jr. et al. | Nov 2015 | A1 |
20150320481 | Cosman, Jr. et al. | Nov 2015 | A1 |
20160030076 | Faller et al. | Feb 2016 | A1 |
20160045248 | Unger et al. | Feb 2016 | A1 |
20160051316 | Boudreaux | Feb 2016 | A1 |
20160074108 | Woodruff et al. | Mar 2016 | A1 |
20160128762 | Harris et al. | May 2016 | A1 |
20160144204 | Akagane | May 2016 | A1 |
20160157927 | Corbett et al. | Jun 2016 | A1 |
20160175029 | Witt et al. | Jun 2016 | A1 |
20160199123 | Thomas et al. | Jul 2016 | A1 |
20160199125 | Jones | Jul 2016 | A1 |
20160206342 | Robertson et al. | Jul 2016 | A1 |
20160262786 | Madan et al. | Sep 2016 | A1 |
20160270840 | Yates et al. | Sep 2016 | A1 |
20160270841 | Strobl et al. | Sep 2016 | A1 |
20160270842 | Strobl et al. | Sep 2016 | A1 |
20160270843 | Boudreaux et al. | Sep 2016 | A1 |
20160278848 | Boudreaux et al. | Sep 2016 | A1 |
20160287311 | Friedrichs | Oct 2016 | A1 |
20160296249 | Robertson | Oct 2016 | A1 |
20160296250 | Olson et al. | Oct 2016 | A1 |
20160296251 | Olson et al. | Oct 2016 | A1 |
20160296252 | Olson et al. | Oct 2016 | A1 |
20160296268 | Gee et al. | Oct 2016 | A1 |
20160296270 | Strobl et al. | Oct 2016 | A1 |
20160317217 | Batross et al. | Nov 2016 | A1 |
20160324537 | Green et al. | Nov 2016 | A1 |
20160338726 | Stulen et al. | Nov 2016 | A1 |
20160346001 | Vakharia et al. | Dec 2016 | A1 |
20160367273 | Robertson et al. | Dec 2016 | A1 |
20160367281 | Gee et al. | Dec 2016 | A1 |
20160374708 | Wiener et al. | Dec 2016 | A1 |
20160374709 | Timm et al. | Dec 2016 | A1 |
20160374712 | Stulen et al. | Dec 2016 | A1 |
20170000512 | Conlon et al. | Jan 2017 | A1 |
20170000516 | Stulen et al. | Jan 2017 | A1 |
20170000541 | Yates et al. | Jan 2017 | A1 |
20170000542 | Yates et al. | Jan 2017 | A1 |
20170000553 | Wiener et al. | Jan 2017 | A1 |
20170000554 | Yates et al. | Jan 2017 | A1 |
20170056056 | Wiener et al. | Mar 2017 | A1 |
20170056058 | Voegele et al. | Mar 2017 | A1 |
20170086876 | Wiener et al. | Mar 2017 | A1 |
20170086908 | Wiener et al. | Mar 2017 | A1 |
20170086909 | Yates et al. | Mar 2017 | A1 |
20170086910 | Wiener et al. | Mar 2017 | A1 |
20170086911 | Wiener et al. | Mar 2017 | A1 |
20170086912 | Wiener et al. | Mar 2017 | A1 |
20170086913 | Yates et al. | Mar 2017 | A1 |
20170095267 | Messerly et al. | Apr 2017 | A1 |
20170105757 | Weir et al. | Apr 2017 | A1 |
20170105782 | Scheib et al. | Apr 2017 | A1 |
20170105786 | Scheib et al. | Apr 2017 | A1 |
20170105791 | Yates et al. | Apr 2017 | A1 |
20170143371 | Witt et al. | May 2017 | A1 |
20170143877 | Witt et al. | May 2017 | A1 |
20170164994 | Smith | Jun 2017 | A1 |
20170189095 | Danziger et al. | Jul 2017 | A1 |
20170189096 | Danziger et al. | Jul 2017 | A1 |
20170196586 | Witt et al. | Jul 2017 | A1 |
20170196587 | Witt et al. | Jul 2017 | A1 |
20170202571 | Shelton, IV et al. | Jul 2017 | A1 |
20170202572 | Shelton, IV et al. | Jul 2017 | A1 |
20170202591 | Shelton, IV et al. | Jul 2017 | A1 |
20170202592 | Shelton, IV et al. | Jul 2017 | A1 |
20170202593 | Shelton, IV et al. | Jul 2017 | A1 |
20170202594 | Shelton, IV et al. | Jul 2017 | A1 |
20170202595 | Shelton, IV | Jul 2017 | A1 |
20170202596 | Shelton, IV et al. | Jul 2017 | A1 |
20170202597 | Shelton, IV et al. | Jul 2017 | A1 |
20170202598 | Shelton, IV et al. | Jul 2017 | A1 |
20170202599 | Shelton, IV et al. | Jul 2017 | A1 |
20170202605 | Shelton, IV et al. | Jul 2017 | A1 |
20170202607 | Shelton, IV et al. | Jul 2017 | A1 |
20170202608 | Shelton, IV et al. | Jul 2017 | A1 |
20170202609 | Shelton, IV et al. | Jul 2017 | A1 |
20170207467 | Shelton, IV et al. | Jul 2017 | A1 |
20170209167 | Nield | Jul 2017 | A1 |
20170238991 | Worrell et al. | Aug 2017 | A1 |
20170245875 | Timm et al. | Aug 2017 | A1 |
20170312014 | Strobl et al. | Nov 2017 | A1 |
20170312015 | Worrell et al. | Nov 2017 | A1 |
20170312016 | Strobl et al. | Nov 2017 | A1 |
20170312017 | Trees et al. | Nov 2017 | A1 |
20170312018 | Trees et al. | Nov 2017 | A1 |
20170312019 | Trees et al. | Nov 2017 | A1 |
20170319228 | Worrell et al. | Nov 2017 | A1 |
20170319265 | Yates et al. | Nov 2017 | A1 |
20170348064 | Stewart et al. | Dec 2017 | A1 |
20180014872 | Dickerson | Jan 2018 | A1 |
20180028257 | Yates et al. | Feb 2018 | A1 |
20180036061 | Yates et al. | Feb 2018 | A1 |
20180036065 | Yates et al. | Feb 2018 | A1 |
20180042658 | Shelton, IV et al. | Feb 2018 | A1 |
20180064961 | Wiener et al. | Mar 2018 | A1 |
20180098785 | Price et al. | Apr 2018 | A1 |
20180098808 | Yates et al. | Apr 2018 | A1 |
20180146976 | Clauda et al. | May 2018 | A1 |
20180177545 | Boudreaux et al. | Jun 2018 | A1 |
20180235691 | Voegele et al. | Aug 2018 | A1 |
20180280083 | Parihar et al. | Oct 2018 | A1 |
20190021783 | Asher et al. | Jan 2019 | A1 |
20190105067 | Boudreaux et al. | Apr 2019 | A1 |
Number | Date | Country |
---|---|---|
2003241752 | Sep 2003 | AU |
2535467 | Apr 1993 | CA |
1233944 | Nov 1999 | CN |
1253485 | May 2000 | CN |
2460047 | Nov 2001 | CN |
1634601 | Jul 2005 | CN |
1640365 | Jul 2005 | CN |
1694649 | Nov 2005 | CN |
1775323 | May 2006 | CN |
1922563 | Feb 2007 | CN |
2868227 | Feb 2007 | CN |
1951333 | Apr 2007 | CN |
101035482 | Sep 2007 | CN |
101040799 | Sep 2007 | CN |
101396300 | Apr 2009 | CN |
101467917 | Jul 2009 | CN |
101474081 | Jul 2009 | CN |
101674782 | Mar 2010 | CN |
101883531 | Nov 2010 | CN |
102160045 | Aug 2011 | CN |
202027624 | Nov 2011 | CN |
102834069 | Dec 2012 | CN |
101313865 | Jan 2013 | CN |
3904558 | Aug 1990 | DE |
9210327 | Nov 1992 | DE |
4300307 | Jul 1994 | DE |
4323585 | Jan 1995 | DE |
19608716 | Apr 1997 | DE |
29623113 | Oct 1997 | DE |
20004812 | Sep 2000 | DE |
20021619 | Mar 2001 | DE |
10042606 | Aug 2001 | DE |
10201569 | Jul 2003 | DE |
102012109037 | Apr 2014 | DE |
0171967 | Feb 1986 | EP |
0336742 | Oct 1989 | EP |
0136855 | Nov 1989 | EP |
0342448 | Nov 1989 | EP |
0443256 | Aug 1991 | EP |
0456470 | Nov 1991 | EP |
0238667 | Feb 1993 | EP |
0340803 | Aug 1993 | EP |
0598976 | Jun 1994 | EP |
0630612 | Dec 1994 | EP |
0424685 | May 1995 | EP |
0677275 | Oct 1995 | EP |
0482195 | Jan 1996 | EP |
0695535 | Feb 1996 | EP |
0705571 | Apr 1996 | EP |
0741996 | Nov 1996 | EP |
0612570 | Jun 1997 | EP |
0557806 | May 1998 | EP |
0640317 | Sep 1999 | EP |
1108394 | Jun 2001 | EP |
1138264 | Oct 2001 | EP |
0908148 | Jan 2002 | EP |
1229515 | Aug 2002 | EP |
0722696 | Dec 2002 | EP |
1285634 | Feb 2003 | EP |
0908155 | Jun 2003 | EP |
0705570 | Apr 2004 | EP |
0765637 | Jul 2004 | EP |
0870473 | Sep 2005 | EP |
0624346 | Nov 2005 | EP |
1594209 | Nov 2005 | EP |
1199044 | Dec 2005 | EP |
1609428 | Dec 2005 | EP |
1199043 | Mar 2006 | EP |
1293172 | Apr 2006 | EP |
0875209 | May 2006 | EP |
1433425 | Jun 2006 | EP |
1256323 | Aug 2006 | EP |
1698289 | Sep 2006 | EP |
1704824 | Sep 2006 | EP |
1749479 | Feb 2007 | EP |
1767157 | Mar 2007 | EP |
1254637 | Aug 2007 | EP |
1815950 | Aug 2007 | EP |
1839599 | Oct 2007 | EP |
1844720 | Oct 2007 | EP |
1862133 | Dec 2007 | EP |
1875875 | Jan 2008 | EP |
1878399 | Jan 2008 | EP |
1915953 | Apr 2008 | EP |
1532933 | May 2008 | EP |
1199045 | Jun 2008 | EP |
1707143 | Jun 2008 | EP |
1943957 | Jul 2008 | EP |
1964530 | Sep 2008 | EP |
1972264 | Sep 2008 | EP |
1974771 | Oct 2008 | EP |
1435852 | Dec 2008 | EP |
1498082 | Dec 2008 | EP |
1707131 | Dec 2008 | EP |
1477104 | Jan 2009 | EP |
2014218 | Jan 2009 | EP |
1849424 | Apr 2009 | EP |
2042112 | Apr 2009 | EP |
2042117 | Apr 2009 | EP |
2060238 | May 2009 | EP |
1832259 | Jun 2009 | EP |
2074959 | Jul 2009 | EP |
1810625 | Aug 2009 | EP |
2090256 | Aug 2009 | EP |
2092905 | Aug 2009 | EP |
2105104 | Sep 2009 | EP |
1747761 | Oct 2009 | EP |
2106758 | Oct 2009 | EP |
2111813 | Oct 2009 | EP |
2131760 | Dec 2009 | EP |
1769766 | Feb 2010 | EP |
2151204 | Feb 2010 | EP |
2153791 | Feb 2010 | EP |
2200145 | Jun 2010 | EP |
1214913 | Jul 2010 | EP |
2238938 | Oct 2010 | EP |
2243439 | Oct 2010 | EP |
2298154 | Mar 2011 | EP |
2305144 | Apr 2011 | EP |
1510178 | Jun 2011 | EP |
1946708 | Jun 2011 | EP |
2335630 | Jun 2011 | EP |
1502551 | Jul 2011 | EP |
1728475 | Aug 2011 | EP |
2353518 | Aug 2011 | EP |
2361562 | Aug 2011 | EP |
2365608 | Sep 2011 | EP |
2420197 | Feb 2012 | EP |
2422721 | Feb 2012 | EP |
1927321 | Apr 2012 | EP |
2436327 | Apr 2012 | EP |
2529681 | Dec 2012 | EP |
1767164 | Jan 2013 | EP |
2316359 | Mar 2013 | EP |
2090238 | Apr 2013 | EP |
2578172 | Apr 2013 | EP |
1586275 | May 2013 | EP |
1616529 | Sep 2013 | EP |
1997438 | Nov 2013 | EP |
2668922 | Dec 2013 | EP |
2508143 | Feb 2014 | EP |
2583633 | Oct 2014 | EP |
2076195 | Dec 2015 | EP |
2113210 | Mar 2016 | EP |
2510891 | Jun 2016 | EP |
2227155 | Jul 2016 | EP |
2859858 | Dec 2016 | EP |
2115068 | Jun 1998 | ES |
1482943 | Aug 1977 | GB |
2032221 | Apr 1980 | GB |
2317566 | Apr 1998 | GB |
2379878 | Nov 2004 | GB |
2472216 | Feb 2011 | GB |
2447767 | Aug 2011 | GB |
S50100891 | Aug 1975 | JP |
S5968513 | May 1984 | JP |
S59141938 | Aug 1984 | JP |
S62221343 | Sep 1987 | JP |
S62227343 | Oct 1987 | JP |
S62292153 | Dec 1987 | JP |
S62292154 | Dec 1987 | JP |
S63109386 | May 1988 | JP |
S63315049 | Dec 1988 | JP |
H01151452 | Jun 1989 | JP |
H01198540 | Aug 1989 | JP |
H0271510 | May 1990 | JP |
H02286149 | Nov 1990 | JP |
H02292193 | Dec 1990 | JP |
H0337061 | Feb 1991 | JP |
H0425707 | Feb 1992 | JP |
H0464351 | Feb 1992 | JP |
H0430508 | Mar 1992 | JP |
H04150847 | May 1992 | JP |
H04152942 | May 1992 | JP |
H 0541716 | Feb 1993 | JP |
H0595955 | Apr 1993 | JP |
H05115490 | May 1993 | JP |
H0670938 | Mar 1994 | JP |
H06104503 | Apr 1994 | JP |
H06217988 | Aug 1994 | JP |
H06507081 | Aug 1994 | JP |
H 07500514 | Jan 1995 | JP |
H07508910 | Oct 1995 | JP |
H07308323 | Nov 1995 | JP |
H0824266 | Jan 1996 | JP |
H08229050 | Sep 1996 | JP |
H08275951 | Oct 1996 | JP |
H08299351 | Nov 1996 | JP |
H08336544 | Dec 1996 | JP |
H08336545 | Dec 1996 | JP |
H09503146 | Mar 1997 | JP |
H09130655 | May 1997 | JP |
H09135553 | May 1997 | JP |
H09140722 | Jun 1997 | JP |
H105237 | Jan 1998 | JP |
H10295700 | Nov 1998 | JP |
H11501543 | Feb 1999 | JP |
H11128238 | May 1999 | JP |
H11192235 | Jul 1999 | JP |
H11253451 | Sep 1999 | JP |
H11318918 | Nov 1999 | JP |
2000041991 | Feb 2000 | JP |
2000070279 | Mar 2000 | JP |
2000210299 | Aug 2000 | JP |
2000271145 | Oct 2000 | JP |
2000287987 | Oct 2000 | JP |
2001029353 | Feb 2001 | JP |
2001502216 | Feb 2001 | JP |
2001309925 | Nov 2001 | JP |
2002059380 | Feb 2002 | JP |
2002177295 | Jun 2002 | JP |
2002186901 | Jul 2002 | JP |
2002204808 | Jul 2002 | JP |
2002238919 | Aug 2002 | JP |
2002263579 | Sep 2002 | JP |
2002301086 | Oct 2002 | JP |
2002306504 | Oct 2002 | JP |
2002330977 | Nov 2002 | JP |
2002542690 | Dec 2002 | JP |
2003000612 | Jan 2003 | JP |
2003010201 | Jan 2003 | JP |
2003510158 | Mar 2003 | JP |
2003116870 | Apr 2003 | JP |
2003126104 | May 2003 | JP |
2003126110 | May 2003 | JP |
2003153919 | May 2003 | JP |
2003530921 | Oct 2003 | JP |
2003310627 | Nov 2003 | JP |
2003339730 | Dec 2003 | JP |
2004129871 | Apr 2004 | JP |
2004147701 | May 2004 | JP |
2005003496 | Jan 2005 | JP |
2005027026 | Jan 2005 | JP |
2005040222 | Feb 2005 | JP |
2005066316 | Mar 2005 | JP |
2005074088 | Mar 2005 | JP |
2005507679 | Mar 2005 | JP |
2005534451 | Nov 2005 | JP |
2005337119 | Dec 2005 | JP |
2006006410 | Jan 2006 | JP |
2006068396 | Mar 2006 | JP |
2006075376 | Mar 2006 | JP |
2006081664 | Mar 2006 | JP |
2006114072 | Apr 2006 | JP |
2006512149 | Apr 2006 | JP |
2006116194 | May 2006 | JP |
2006158525 | Jun 2006 | JP |
2006217716 | Aug 2006 | JP |
2006218296 | Aug 2006 | JP |
2006288431 | Oct 2006 | JP |
2007037568 | Feb 2007 | JP |
2007050181 | Mar 2007 | JP |
2007-524459 | Aug 2007 | JP |
2007229454 | Sep 2007 | JP |
2007527747 | Oct 2007 | JP |
2007296369 | Nov 2007 | JP |
200801876 | Jan 2008 | JP |
2008018226 | Jan 2008 | JP |
200833644 | Feb 2008 | JP |
2008036390 | Feb 2008 | JP |
2008508065 | Mar 2008 | JP |
2008119250 | May 2008 | JP |
2008515562 | May 2008 | JP |
2008521503 | Jun 2008 | JP |
2008188160 | Aug 2008 | JP |
D1339835 | Aug 2008 | JP |
2008212679 | Sep 2008 | JP |
2008536562 | Sep 2008 | JP |
2008284374 | Nov 2008 | JP |
2009511206 | Mar 2009 | JP |
2009082711 | Apr 2009 | JP |
2009517181 | Apr 2009 | JP |
4262923 | May 2009 | JP |
2009523567 | Jun 2009 | JP |
2009148557 | Jul 2009 | JP |
2009236177 | Oct 2009 | JP |
2009254819 | Nov 2009 | JP |
2010000336 | Jan 2010 | JP |
2010009686 | Jan 2010 | JP |
2010514923 | May 2010 | JP |
2010121865 | Jun 2010 | JP |
2010534522 | Nov 2010 | JP |
2010540186 | Dec 2010 | JP |
2011505198 | Feb 2011 | JP |
2012075899 | Apr 2012 | JP |
2012071186 | Apr 2012 | JP |
2012235658 | Nov 2012 | JP |
5208761 | Jun 2013 | JP |
5714508 | May 2015 | JP |
2015515339 | May 2015 | JP |
5836543 | Dec 2015 | JP |
100789356 | Dec 2007 | KR |
2154437 | Aug 2000 | RU |
22035 | Mar 2002 | RU |
2201169 | Mar 2003 | RU |
2304934 | Aug 2007 | RU |
2405603 | Dec 2010 | RU |
850068 | Jul 1981 | SU |
WO-8103272 | Nov 1981 | WO |
WO-9222259 | Dec 1992 | WO |
WO-9307817 | Apr 1993 | WO |
WO-9308757 | May 1993 | WO |
WO-9314708 | Aug 1993 | WO |
WO-9316646 | Sep 1993 | WO |
WO-9320877 | Oct 1993 | WO |
WO-9322973 | Nov 1993 | WO |
WO-9400059 | Jan 1994 | WO |
WO-9421183 | Sep 1994 | WO |
WO-9424949 | Nov 1994 | WO |
WO-9509572 | Apr 1995 | WO |
WO-9510978 | Apr 1995 | WO |
WO-9534259 | Dec 1995 | WO |
WO-9630885 | Oct 1996 | WO |
WO-9635382 | Nov 1996 | WO |
WO-9639086 | Dec 1996 | WO |
WO-9710764 | Mar 1997 | WO |
WO-9800069 | Jan 1998 | WO |
WO-9816156 | Apr 1998 | WO |
WO-9826739 | Jun 1998 | WO |
WO-9835621 | Aug 1998 | WO |
WO-9837815 | Sep 1998 | WO |
WO-9840020 | Sep 1998 | WO |
WO-9847436 | Oct 1998 | WO |
WO-9857588 | Dec 1998 | WO |
WO-9920213 | Apr 1999 | WO |
WO-9923960 | May 1999 | WO |
WO-9940857 | Aug 1999 | WO |
WO-9940861 | Aug 1999 | WO |
WO-9952489 | Oct 1999 | WO |
WO-0024330 | May 2000 | WO |
WO-0024331 | May 2000 | WO |
WO-0025691 | May 2000 | WO |
WO-0064358 | Nov 2000 | WO |
WO-0074585 | Dec 2000 | WO |
WO-0124713 | Apr 2001 | WO |
WO-0128444 | Apr 2001 | WO |
WO-0154590 | Aug 2001 | WO |
WO-0167970 | Sep 2001 | WO |
WO-0172251 | Oct 2001 | WO |
WO-0195810 | Dec 2001 | WO |
WO-0224080 | Mar 2002 | WO |
WO-0238057 | May 2002 | WO |
WO-02062241 | Aug 2002 | WO |
WO-02080797 | Oct 2002 | WO |
WO-03001986 | Jan 2003 | WO |
WO-03013374 | Feb 2003 | WO |
WO-03020339 | Mar 2003 | WO |
WO-03028541 | Apr 2003 | WO |
WO-03030708 | Apr 2003 | WO |
WO-03068046 | Aug 2003 | WO |
WO-03082133 | Oct 2003 | WO |
WO-03095028 | Nov 2003 | WO |
WO-2004011037 | Feb 2004 | WO |
WO-2004012615 | Feb 2004 | WO |
WO-2004026104 | Apr 2004 | WO |
WO-2004032754 | Apr 2004 | WO |
WO-2004032762 | Apr 2004 | WO |
WO-2004032763 | Apr 2004 | WO |
WO-2004037095 | May 2004 | WO |
WO-2004060141 | Jul 2004 | WO |
WO-2004078051 | Sep 2004 | WO |
WO-2004098426 | Nov 2004 | WO |
WO-2004112618 | Dec 2004 | WO |
WO-2005052959 | Jun 2005 | WO |
WO-2005117735 | Dec 2005 | WO |
WO-2005122917 | Dec 2005 | WO |
WO-2006012797 | Feb 2006 | WO |
WO-2006021269 | Mar 2006 | WO |
WO-2006036706 | Apr 2006 | WO |
WO-2006042210 | Apr 2006 | WO |
WO-2006055166 | May 2006 | WO |
WO-2006058223 | Jun 2006 | WO |
WO-2006063199 | Jun 2006 | WO |
WO-2006083988 | Aug 2006 | WO |
WO-2006101661 | Sep 2006 | WO |
WO-2006119139 | Nov 2006 | WO |
WO-2006119376 | Nov 2006 | WO |
WO-2006129465 | Dec 2006 | WO |
WO-2007008703 | Jan 2007 | WO |
WO-2007008710 | Jan 2007 | WO |
WO-2007038538 | Apr 2007 | WO |
WO-2007040818 | Apr 2007 | WO |
WO-2007047380 | Apr 2007 | WO |
WO-2007047531 | Apr 2007 | WO |
WO-2007056590 | May 2007 | WO |
WO-2007087272 | Aug 2007 | WO |
WO-2007089724 | Aug 2007 | WO |
WO-2007143665 | Dec 2007 | WO |
WO-2008016886 | Feb 2008 | WO |
WO-2008020964 | Feb 2008 | WO |
WO-2008042021 | Apr 2008 | WO |
WO-2008045348 | Apr 2008 | WO |
WO-2008049084 | Apr 2008 | WO |
WO-2008051764 | May 2008 | WO |
WO-2008089174 | Jul 2008 | WO |
WO-2008099529 | Aug 2008 | WO |
WO-2008101356 | Aug 2008 | WO |
WO-2008118709 | Oct 2008 | WO |
WO-2008130793 | Oct 2008 | WO |
WO-2009010565 | Jan 2009 | WO |
WO-2009018067 | Feb 2009 | WO |
WO-2009018406 | Feb 2009 | WO |
WO-2009022614 | Feb 2009 | WO |
WO-2009027065 | Mar 2009 | WO |
WO-2009036818 | Mar 2009 | WO |
WO-2009039179 | Mar 2009 | WO |
WO-2009046234 | Apr 2009 | WO |
WO-2009059741 | May 2009 | WO |
WO-2009073402 | Jun 2009 | WO |
WO-2009082477 | Jul 2009 | WO |
WO-2009088550 | Jul 2009 | WO |
WO-2009120992 | Oct 2009 | WO |
WO-2009141616 | Nov 2009 | WO |
WO-2009149234 | Dec 2009 | WO |
WO-2010017149 | Feb 2010 | WO |
WO-2010017266 | Feb 2010 | WO |
WO-2010068783 | Jun 2010 | WO |
WO-2010104755 | Sep 2010 | WO |
WO-2011008672 | Jan 2011 | WO |
WO-2011044338 | Apr 2011 | WO |
WO-2011044343 | Apr 2011 | WO |
WO-2011052939 | May 2011 | WO |
WO-2011060031 | May 2011 | WO |
WO-2011084768 | Jul 2011 | WO |
WO-2011089717 | Jul 2011 | WO |
WO-2011100321 | Aug 2011 | WO |
WO-2011144911 | Nov 2011 | WO |
WO-2012044597 | Apr 2012 | WO |
WO-2012044606 | Apr 2012 | WO |
WO-2012061638 | May 2012 | WO |
WO-2012061722 | May 2012 | WO |
WO-2012128362 | Sep 2012 | WO |
WO-2012135705 | Oct 2012 | WO |
WO-2012135721 | Oct 2012 | WO |
WO-2012150567 | Nov 2012 | WO |
WO-2012166510 | Dec 2012 | WO |
WO-2013018934 | Feb 2013 | WO |
WO-2013034629 | Mar 2013 | WO |
WO-2013062978 | May 2013 | WO |
WO-2013102602 | Jul 2013 | WO |
WO-2013154157 | Oct 2013 | WO |
WO-2014092108 | Jun 2014 | WO |
WO-2015197395 | Dec 2015 | WO |
WO-2016009921 | Jan 2016 | WO |
WO-2016091400 | Jun 2016 | WO |
Entry |
---|
Weir, C.E., “Rate of shrinkage of tendon collagen—heat, entropy and free energy of activation of the shrinkage of untreated tendon. Effect of acid salt, pickle, and tannage on the activation of tendon collagen.” Journal of the American Leather Chemists Association, 44, pp. 108-140 (1949). |
Henriques. F.C., “Studies in thermal injury V. The predictability and the significance of thermally induced rate processes leading to irreversible epidermal injury.” Archives of Pathology, 434, pp. 489-502 (1947). |
Arnoczky et al., “Thermal Modification of Conective Tissues: Basic Science Considerations and Clinical Implications,” J. Am Acad Orthop Surg, vol. 8, No. 5, pp. 305-313 (Sep./Oct. 2000). |
Chen et al., “Heat-Induced Changes in the Mechanics of a Collagenous Tissue: Isothermal Free Shrinkage,” Transactions of the ASME, vol. 119, pp. 372-378 (Nov. 1997). |
Chen et al., “Heat-Induced Changes in the Mechanics of a Collagenous Tissue: Isothermal, Isotonic Shrinkage,” Transactions of the ASME, vol. 120, pp. 382-388 (Jun. 1998). |
Chen et al., “Phenomenological Evolution Equations for Heat-Induced Shrinkage of a Collagenous Tissue,” IEEE Transactions on Biomedical Engineering, vol. 45, No. 10, pp. 1234-1240 (Oct. 1998). |
Harris et al., “Kinetics of Thermal Damage to a Collagenous Membrane Under Biaxial Isotonic Loading,” IEEE Transactions on Biomedical Engineering, vol. 51, No. 2, pp. 371-379 (Feb. 2004). |
Harris et al., “Altered Mechanical Behavior of Epicardium Due to Isothermal Heating Under Biaxial Isotonic Loads,” Journal of Biomechanical Engineering, vol. 125, pp. 381-388 (Jun. 2003). |
Lee et al., “A multi-sample denaturation temperature tester for collagenous biomaterials,” Med. Eng. Phy., vol. 17, No. 2, pp. 115-121 (Mar. 1995). |
Moran et al., “Thermally Induced Shrinkage of Joint Capsule,” Clinical Orthopaedics and Related Research, No. 281, pp. 248-255 (Dec. 2000). |
Wall et al., “Thermal modification of collagen,” J Shoulder Elbow Surg, No. 8, pp. 339-344 (Jul./Aug. 1999). |
Wells et al., “Altered Mechanical Behavior of Epicardium Under Isothermal Biaxial Loading,” Transactions of the ASME, Journal of Biomedical Engineering, vol. 126, pp. 492-497 (Aug. 2004). |
Gibson, “Magnetic Refrigerator Successfully Tested,” U.S. Department of Energy Research News, accessed online on Aug. 6, 2010 at http://www.eurekalert.org/features/doe/2001-11/dl-mrs062802.php (Nov. 1, 2001). |
Humphrey, J.D., “Continuum Thermomechanics and the Clinical Treatment of Disease and Injury,” Appl. Mech. Rev., vol. 56, No. 2 pp. 231-260 (Mar. 2003). |
National Semiconductors Temperature Sensor Handbook—http://www.national.com/appinfo/tempsensors/files/temphb.pdf; accessed online: Apr. 1, 2011. |
Hayashi et al., “The Effect of Thermal Heating on the Length and Histologic Properties of the Glenohumeral Joint Capsule,” American Journal of Sports Medicine, vol. 25, Issue 1, 11 pages (Jan. 1997), URL: http://www.mdconsult.com/das/article/body/156183648-2/jorg=journal&source=MI&sp=1 . . . , accessed Aug. 25, 2009. |
Douglas, S.C. “Introduction to Adaptive Filter”. Digital Signal Processing Handbook. Ed. Vijay K. Madisetti and Douglas B. Williams. Boca Raton: CRC Press LLC, 1999. |
Chen et al., “Heat-induced changes in the mechanics of a collagenous tissue: pseudoelastic behavior at 37° C.,” Journal of Biomechanics, 31, pp. 211-216 (1998). |
Kurt Gieck & Reiner Gieck, Engineering Formulas § Z.7 (7th ed. 1997). |
Glaser and Subak-Sharpe,Integrated Circuit Engineering, Addison-Wesley Publishing, Reading, MA (1979). (book—not attached). |
Wright, et al., “Time-Temperature Equivalence of Heat-Induced Changes in Cells and Proteins,” Feb. 1998. ASME Journal of Biomechanical Engineering, vol. 120, pp. 22-26. |
Covidien Brochure, [Value Analysis Brief], LigaSure Advance™ Pistol Grip, dated Rev. Apr. 2010 (7 pages). |
Covidien Brochure, LigaSure Impact™ Instrument LF4318, dated Feb. 2013 (3 pages). |
Covidien Brochure, LigaSure Atlas™ Hand Switching Instruments, dated Dec. 2008 (2 pages). |
Covidien Brochure, The LigaSure™ 5 mm Blunt Tip Sealer/Divider Family, dated Apr. 2013 (2 pages). |
Sullivan, “Optimal Choice for Number of Strands in a Litz-Wire Transformer Winding,” IEEE Transactions on Power Electronics, vol. 14, No. 2, Mar. 1999, pp. 283-291. |
Covidien Brochure, The LigaSure Precise™ Instrument, dated Mar. 2011 (2 pages). |
https://www.kjmagnetics.com/fieldcalculator.asp, retrieved Jul. 11, 2016, backdated to Nov. 11, 2011 via https://web.archive.org/web/20111116164447/http://www.kjmagnetics.com/fieldcalculator.asp. |
Leonard I. Malis, M.D., “The Value of Irrigation During Bipolar Coagulation,” 1989. |
Jang, J. et al. “Neuro-fuzzy and Soft Computing.” Prentice Hall, 1997, pp. 13-89, 199-293, 335-393, 453-496, 535-549. |
AST Products, Inc., “Principles of Video Contact Angle Analysis,” 20 pages, (2006). |
Lim et al., “A Review of Mechanism Used in Laparoscopic Surgical Instruments,” Mechanism and Machine Theory, vol. 38, pp. 1133-1147, (2003). |
F. A. Duck, “Optical Properties of Tissue Including Ultraviolet and Infrared Radiation,” pp. 43-71 in Physical Properties of Tissue (1990). |
Erbe Electrosurgery VIO® 200 S, (2012), p. 7, 12 pages, accessed Mar. 31, 2014 at http://www.erbe-med. com/erbe/media/Marketing materialien/85140170 ERBE EN VIO 200 S D027541. |
Graff, K.F., “Elastic Wave Propagation in a Curved Sonic Transmission Line,” IEEE Transactions on Sonics and Ultrasonics, SU-17(1), 1-6 (1970). |
Makarov, S. N., Ochmann, M., Desinger, K., “The longitudinal vibration response of a curved fiber used for laser ultrasound surgical therapy,” Journal of the Acoustical Society of America 102, 1191-1199 (1997). |
Morley, L. S. D., “Elastic Waves in a Naturally Curved Rod,” Quarterly Journal of Mechanics and Applied Mathematics, 14: 155-172 (1961). |
Walsh, S. J., White, R. G., “Vibrational Power Transmission in Curved Beams,” Journal of Sound and Vibration, 233(3), 455-488 (2000). |
Covidien 501(k) Summary Sonicision, dated Feb. 24, 2011 (7 pages). |
http://www.apicalinstr.com/generators.htm. |
http://www.dotmed.com/listing/electrosurical-unit/ethicon/ultracision-g110-/1466724. |
http:/www.ethicon.com/gb-en/healthcare-professionals/products/energy-devices/capital//ge . . . . |
http://www.medicalexpo.com/medical-manufacturer/electrosurgical-generator-6951.html. |
http://www.megadyne.com/es_generator.php. |
http://www.valleylab.com/product/es/generators/index.html. |
Gerhard, Glen C., “Surgical Electrotechnology: Quo Vadis?,” IEEE Transactions on Biomedical Engineering, vol. BME-31, No. 12, pp. 787-792, Dec. 1984. |
Technology Overview, printed from www.harmonicscalpel.com, Internet site, website accessed on Jun. 13, 2007, (3 pages). |
Sherrit et al., “Novel Horn Designs for Ultrasonic/Sonic Cleaning Welding, Soldering, Cutting and Drilling,” Proc. SPIE Smart Structures Conference, vol. 4701, Paper No. 34, San Diego, CA, pp. 353-360, Mar. 2002. |
Gooch et al., “Recommended Infection-Control Practices for Dentistry, 1993,” Published: May 28, 1993; [retrieved on Aug. 23, 2008]. Retrieved from the internet: URL: http//wonder.cdc.gov/wonder/prevguid/p0000191/p0000191.asp (15 pages). |
Huston et al., “Magnetic and Magnetostrictive Properties of Cube Textured Nickel for Magnetostrictive Transducer Applications,” IEEE Transactions on Magnetics, vol. 9(4), pp. 636-640 (Dec. 1973). |
Sullivan, “Cost-Constrained Selection of Strand Diameter and Number in a Litz-Wire Transformer Winding,” IEEE Transactions on Power Electronics, vol. 16, No. 2, Mar. 2001, pp. 281-288. |
Fowler, K.R., “A Programmable, Arbitrary Waveform Electrosurgical Device,” IEEE Engineering in Medicine and Biology Society 10th Annual International Conference, pp. 1324, 1325 (1988). |
LaCourse, J.R.; Vogt, M.C.; Miller, W.T., III; Selikowitz, S.M., “Spectral Analysis Interpretation of Electrosurgical Generator Nerve and Muscle Stimulation,” IEEE Transactions on Biomedical Engineering, vol. 35, No. 7, pp. 505-509, Jul. 1988. |
Orr et al., “Overview of Bioheat Transfer,” pp. 367-384 in Optical-Thermal Response of Laser-Irradiated Tissue, A. J. Welch and M. J. C. van Gernert, eds., Plenum, New York (1995). |
Campbell et al, “Thermal Imaging in Surgery,” p. 19-3, in Medical Infrared Imaging, N. A. Diakides and J. D. Bronzino, Eds. (2008). |
http://www.4-traders.com/JOHNSON-JOHNSON-4832/news/Johnson-Johnson-Ethicon-E . . . . |
Incropera et al., Fundamentals of Heat and Mass Transfer, Wiley, New York (1990). (Book—not attached). |
Hörmann et al., “Reversible and irreversible denaturation of collagen fibers.” Biochemistry, 10, pp. 932-937 (1971). |
Dean, D.A., “Electrical Impedance Spectroscopy Study of Biological Tissues,” J. Electrostat, 66(3-4), Mar. 2008, pp. 165-177. Accessed Apr. 10, 2018: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2597841/. |
Moraleda et al., A Temperature Sensor Based on a Polymer Optical Fiber Macro-Bend, Sensors 2013, 13, 13076-13089, doi: 10.3390/s131013076, ISSN 1424-8220. |
Number | Date | Country | |
---|---|---|---|
20170086914 A1 | Mar 2017 | US |
Number | Date | Country | |
---|---|---|---|
62235368 | Sep 2015 | US | |
62235260 | Sep 2015 | US | |
62235466 | Sep 2015 | US |