Apparatus and method for differentiating between tissue and mechanical obstruction in a surgical instrument

Abstract
A surgical instrument is provided. The surgical instrument includes: a handle assembly; a jaw assembly comprising a staple cartridge containing a plurality of staples and an anvil to form the plurality of staples upon firing; a drive assembly at least partially located within the handle and connected to the jaw assembly and the lockout mechanism; a motor disposed within the handle assembly and operatively coupled to the drive assembly; and a controller operatively coupled to the motor, the controller configured to control supply of electrical current to the motor and to monitor a current draw of the motor, wherein the controller is further configured to terminate the supply of electrical current to the motor in response to a rate of change of the current draw indicative of a mechanical limit of at least one of the jaw assembly, the drive assembly, or the motor.
Description
BACKGROUND

1. Technical Field


The present disclosure relates to surgical apparatuses, devices and/or systems for performing endoscopic surgical procedures and methods of use thereof. More specifically, the present disclosure relates to electromechanical, hand-held surgical apparatus, devices and/or systems configured for use with removable disposable end effectors and/or single use end effectors for clamping, cutting and/or stapling tissue.


2. Background of the Related Art


A number of surgical device manufacturers have developed product lines with proprietary drive systems for operating and/or manipulating electromechanical surgical devices. In many instances the electromechanical surgical devices include a reusable handle assembly, and disposable or single use end effectors. The end effectors are selectively connected to the handle assembly prior to use and then disconnected from the handle assembly following use in order to be disposed of or in some instances sterilized for re-use.


Many of these electromechanical surgical devices include complex drive components that utilize a variety of user interfaces that accept user inputs (e.g., controls) for controlling the devices as well as provide feedback to the user. To prevent actuation of drive mechanisms beyond mechanical limits, various switches and sensors are used to detect operational state of the surgical devices. Inclusion of multiple switches and/or sensors in the devices as well as end effectors presents various problems. In addition, cost or other considerations prevent the use of such devices. Accordingly, there is a need for systems and apparatuses having safety mechanisms that can detect mechanical limits without relying on multiple mechanical limit sensors and/or switches disposed throughout the surgical device.


SUMMARY

According to one embodiment of the present disclosure a surgical instrument is provided. The surgical instrument includes: a handle assembly; a jaw assembly including a staple cartridge containing a plurality of staples and an anvil to form the plurality of staples upon firing; a drive assembly at least partially located within the handle and connected to the jaw assembly and the lockout mechanism; a motor disposed within the handle assembly and operatively coupled to the drive assembly; and a controller operatively coupled to the motor, the controller configured to control supply of electrical current to the motor and to monitor a current draw of the motor, wherein the controller is further configured to terminate the supply of electrical current to the motor in response to a rate of change of the current draw indicative of a mechanical limit of at least one of the jaw assembly, the drive assembly, or the motor.


According to one aspect of the above embodiment, the controller is further configured to determine if motor current is unstable by determining whether the rate of change of the current draw is outside a first range.


According to one aspect of the above embodiment, the controller is further configured to determine if motor current is stable by determining whether the rate of change of the current draw is within a second range, wherein the second range is within the first range.


According to one aspect of the above embodiment, the controller is further configured to store a stability counter of current draw samples within the second range.


According to one aspect of the above embodiment, the controller determines whether motor current is stable if the stability counter is above a predetermined stability threshold.


According to one aspect of the above embodiment, the controller is further configured to determine if the motor reached the mechanical limit by determining whether the motor current is stable and the rate of change of the current draw is within a third range.


According to one aspect of the above embodiment, the third range is within the first range and is higher than the second range.


According to one aspect of the above embodiment, the controller is further configured to store an event counter of current draw samples within the third range.


According to one aspect of the above embodiment, the controller determines whether the motor reached the mechanical limit if the event counter is above a predetermined event threshold.


According to another embodiment of the present disclosure a surgical instrument is provided. The surgical instrument includes: a handle assembly; a jaw assembly including a staple cartridge containing a plurality of staples and an anvil to form the plurality of staples upon firing; a drive assembly at least partially located within the handle and connected to the jaw assembly and the lockout mechanism; a motor disposed within the handle assembly and operatively coupled to the drive assembly; and a controller operatively coupled to the motor, the controller to determine whether the motor has reached a mechanical limit based on a rate of change of a current draw by the motor indicative of the mechanical limit.


According to one aspect of the above embodiment, the controller is further configured to determine whether motor current is unstable by determining whether the rate of change of the current draw is outside a first range.


According to one aspect of the above embodiment, the controller is further configured to determine whether motor current is stable by determining whether a plurality of samples of the rate of change of the current draw are within a second range.


According to one aspect of the above embodiment, the controller is further configured to store a stability counter of current draw samples within the second range.


According to one aspect of the above embodiment, the controller determines whether motor current is stable if the stability counter is above a predetermined stability threshold.


According to one aspect of the above embodiment, the controller is further configured to determine whether the motor reached the mechanical limit by determining whether the motor current is stable and a plurality of samples of the rate of change of the current draw are within a third range.


According to one aspect of the above embodiment, the second and third ranges are within the first range and the third range is higher than the second range.


According to one aspect of the above embodiment, the controller is further configured to store an event counter of current draw samples within the third range.


According to one aspect of the above embodiment, the controller determines whether the motor reached the mechanical limit if the event counter is above a predetermined event threshold.


According to a further embodiment of the present disclosure a method for controlling a surgical instrument is provided. The method includes: monitoring a current draw of a motor coupled to a drive assembly for actuating a jaw assembly; calculating a rate of change of the current draw; and determining whether the motor has reached a mechanical limit based on the rate of change of the current draw by the motor.


According to one aspect of the above embodiment, the method further includes determining whether the rate of change of the current draw is outside a first range to determine whether motor current is unstable.


According to one aspect of the above embodiment, the method further includes determining whether a plurality of samples of the rate of change of the current draw are within a second range to determine whether motor current is stable.


According to one aspect of the above embodiment, the method further includes: storing a stability counter of current draw samples within the second range; and determining whether motor current is stable if the stability counter is above a predetermined stability threshold.


According to one aspect of the above embodiment, the method further includes: whether the motor current is stable and a plurality of samples of the rate of change of the current draw are within a third range to determine whether the motor reached the mechanical limit by.


According to one aspect of the above embodiment, the second and third ranges are within the first range and the third range is higher than the second range.


According to one aspect of the above embodiment, the method further includes: storing an event counter of current draw samples within the third range; and determining whether the motor reached the mechanical limit if the event counter is above a predetermined event threshold.





DESCRIPTION OF THE DRAWINGS

Embodiments of the present disclosure are described herein with reference to the accompanying drawings, wherein:



FIG. 1 is a perspective, disassembled view of an electromechanical surgical system including a surgical instrument, an adapter, and an end effector, according to the present disclosure;



FIG. 2 is a perspective view of the surgical instrument of FIG. 1, according to the present disclosure;



FIG. 3 is perspective, exploded view of the surgical instrument of FIG. 1, according to the present disclosure;



FIG. 4 is a perspective view of a battery of the surgical instrument of FIG. 1, according to the present disclosure;



FIG. 5 is a top, partially-disassembled view of the surgical instrument of FIG. 1, according to the present disclosure;



FIG. 6 is a front, perspective view of the surgical instrument of FIG. 1 with the adapter separated therefrom, according to the present disclosure;



FIG. 7 is a side, cross-sectional view of the surgical instrument of FIG. 1, as taken through 7-7 of FIG. 2, according to the present disclosure;



FIG. 8 is a top, cross-sectional view of the surgical instrument of FIG. 1, as taken through 8-8 of FIG. 2, according to the present disclosure;



FIG. 9 is a perspective, exploded view of a end effector of FIG. 1, according to the present disclosure;



FIG. 10 is a schematic diagram of the surgical instrument of FIG. 1 according to the present disclosure;



FIG. 11 is a schematic diagram of motor current values stored in memory of the surgical instrument of FIG. 1 according to the present disclosure;



FIG. 12 is a flow chart of a method for controlling the surgical instrument of FIG. 1 according to the present disclosure;



FIGS. 13-15 are plots of motor current of the surgical instrument as controlled by the method of the present disclosure; and



FIG. 16 is a flow chart of a method for controlling the surgical instrument of FIG. 1 according to another embodiment of the present disclosure.





DETAILED DESCRIPTION

A surgical system, in accordance with an embodiment of the present disclosure, is generally designated as 10, and is in the form of a powered hand held electromechanical instrument configured for selective attachment thereto of a plurality of different end effectors that are each configured for actuation and manipulation by the powered hand held electromechanical surgical instrument.


As illustrated in FIG. 1, surgical instrument 100 is configured for selective connection with an adapter 200, and, in turn, adapter 200 is configured for selective connection with an end effector or single use loading unit 300.


As illustrated in FIGS. 1-3, surgical instrument 100 includes a handle housing 102 having a lower housing portion 104, an intermediate housing portion 106 extending from and/or supported on lower housing portion 104, and an upper housing portion 108 extending from and/or supported on intermediate housing portion 106. Intermediate housing portion 106 and upper housing portion 108 are separated into a distal half-section 110a that is integrally formed with and extending from the lower portion 104, and a proximal half-section 110b connectable to distal half-section 110a by a plurality of fasteners. When joined, distal and proximal half-sections 110a, 110b define a handle housing 102 having a cavity 102a therein in which a circuit board 150 and a drive mechanism 160 is situated.


Distal and proximal half-sections 110a, 110b are divided along a plane that traverses a longitudinal axis “X” of upper housing portion 108, as seen in FIGS. 2 and 3. Handle housing 102 includes a gasket 112 extending completely around a rim of distal half-section and/or proximal half-section 110a, 110b and being interposed between distal half-section 110a and proximal half-section 110b. Gasket 112 seals the perimeter of distal half-section 110a and proximal half-section 110b. Gasket 112 functions to establish an air-tight seal between distal half-section 110a and proximal half-section 110b such that circuit board 150 and drive mechanism 160 are protected from sterilization and/or cleaning procedures.


In this manner, the cavity 102a of handle housing 102 is sealed along the perimeter of distal half-section 110a and proximal half-section 110b yet is configured to enable easier, more efficient assembly of circuit board 150 and a drive mechanism 160 in handle housing 102.


Intermediate housing portion 106 of handle housing 102 provides a housing in which circuit board 150 is situated. Circuit board 150 is configured to control the various operations of surgical instrument 100, as will be set forth in additional detail below.


Lower housing portion 104 of surgical instrument 100 defines an aperture (not shown) formed in an upper surface thereof and which is located beneath or within intermediate housing portion 106. The aperture of lower housing portion 104 provides a passage through which wires 152 pass to electrically interconnect electrical components (a battery 156, as illustrated in FIG. 4, a circuit board 154, as illustrated in FIG. 3, etc.) situated in lower housing portion 104 with electrical components (circuit board 150, drive mechanism 160, etc.) situated in intermediate housing portion 106 and/or upper housing portion 108.


Handle housing 102 includes a gasket 103 disposed within the aperture of lower housing portion 104 (not shown) thereby plugging or sealing the aperture of lower housing portion 104 while allowing wires 152 to pass therethrough. Gasket 103 functions to establish an air-tight seal between lower housing portion 106 and intermediate housing portion 108 such that circuit board 150 and drive mechanism 160 are protected from sterilization and/or cleaning procedures.


As shown, lower housing portion 104 of handle housing 102 provides a housing in which a rechargeable battery 156, is removably situated. Battery 156 is configured to supply power to any of the electrical components of surgical instrument 100. Lower housing portion 104 defines a cavity (not shown) into which battery 156 is inserted. Lower housing portion 104 includes a door 105 pivotally connected thereto for closing cavity of lower housing portion 104 and retaining battery 156 therein.


With reference to FIGS. 3 and 5, distal half-section 110a of upper housing portion 108 defines a nose or connecting portion 108a. A nose cone 114 is supported on nose portion 108a of upper housing portion 108. Nose cone 114 is fabricated from a transparent material. An illumination member 116 is disposed within nose cone 114 such that illumination member 116 is visible therethrough. Illumination member 116 is may be a light emitting diode printed circuit board (LED PCB). Illumination member 116 is configured to illuminate multiple colors with a specific color pattern being associated with a unique discrete event.


Upper housing portion 108 of handle housing 102 provides a housing in which drive mechanism 160 is situated. As illustrated in FIG. 5, drive mechanism 160 is configured to drive shafts and/or gear components in order to perform the various operations of surgical instrument 100. In particular, drive mechanism 160 is configured to drive shafts and/or gear components in order to selectively move tool assembly 304 of end effector 300 (see FIGS. 1 and 9) relative to proximal body portion 302 of end effector 300, to rotate end effector 300 about a longitudinal axis “X” (see FIG. 2) relative to handle housing 102, to move anvil assembly 306 relative to cartridge assembly 308 of end effector 300, and/or to fire a stapling and cutting cartridge within cartridge assembly 308 of end effector 300.


The drive mechanism 160 includes a selector gearbox assembly 162 that is located immediately proximal relative to adapter 200. Proximal to the selector gearbox assembly 162 is a function selection module 163 having a first motor 164 that functions to selectively move gear elements within the selector gearbox assembly 162 into engagement with an input drive component 165 having a second motor 166.


As illustrated in FIGS. 1-4, and as mentioned above, distal half-section 110a of upper housing portion 108 defines a connecting portion 108a configured to accept a corresponding drive coupling assembly 210 of adapter 200.


As illustrated in FIGS. 6-8, connecting portion 108a of surgical instrument 100 has a cylindrical recess 108b that receives a drive coupling assembly 210 of adapter 200 when adapter 200 is mated to surgical instrument 100. Connecting portion 108a houses three rotatable drive connectors 118, 120, 122.


When adapter 200 is mated to surgical instrument 100, each of rotatable drive connectors 118, 120, 122 of surgical instrument 100 couples with a corresponding rotatable connector sleeve 218, 220, 222 of adapter 200 as shown in FIG. 6. In this regard, the interface between corresponding first drive connector 118 and first connector sleeve 218, the interface between corresponding second drive connector 120 and second connector sleeve 220, and the interface between corresponding third drive connector 122 and third connector sleeve 222 are keyed such that rotation of each of drive connectors 118, 120, 122 of surgical instrument 100 causes a corresponding rotation of the corresponding connector sleeve 218, 220, 222 of adapter 200.


The mating of drive connectors 118, 120, 122 of surgical instrument 100 with connector sleeves 218, 220, 222 of adapter 200 allows rotational forces to be independently transmitted via each of the three respective connector interfaces. The drive connectors 118, 120, 122 of surgical instrument 100 are configured to be independently rotated by drive mechanism 160. In this regard, the function selection module 163 of drive mechanism 160 selects which drive connector or connectors 118, 120, 122 of surgical instrument 100 is to be driven by the input drive component 165 of drive mechanism 160.


Since each of drive connectors 118, 120, 122 of surgical instrument 100 has a keyed and/or substantially non-rotatable interface with respective connector sleeves 218, 220, 222 of adapter 200, when adapter 200 is coupled to surgical instrument 100, rotational force(s) are selectively transferred from drive mechanism 160 of surgical instrument 100 to adapter 200.


The selective rotation of drive connector(s) 118, 120 and/or 122 of surgical instrument 100 allows surgical instrument 100 to selectively actuate different functions of end effector 300. As will be discussed in greater detail below, selective and independent rotation of first drive connector 118 of surgical instrument 100 corresponds to the selective and independent opening and closing of tool assembly 304 of end effector 300, and driving of a stapling/cutting component of tool assembly 304 of end effector 300. Also, the selective and independent rotation of second drive connector 120 of surgical instrument 100 corresponds to the selective and independent articulation of tool assembly 304 of end effector 300 transverse to longitudinal axis “X” (see FIG. 2). Additionally, the selective and independent rotation of third drive connector 122 of surgical instrument 100 corresponds to the selective and independent rotation of end effector 300 about longitudinal axis “X” (see FIG. 2) relative to handle housing 102 of surgical instrument 100.


As mentioned above and as illustrated in FIGS. 5 and 8, drive mechanism 160 includes a selector gearbox assembly 162; and a function selection module 163, located proximal to the selector gearbox assembly 162, that functions to selectively move gear elements within the selector gearbox assembly 162 into engagement with second motor 166. Thus, drive mechanism 160 selectively drives one of drive connectors 118, 120, 122 of surgical instrument 100 at a given time.


As illustrated in FIGS. 1-3, handle housing 102 supports a control assembly 107 on a distal surface or side of intermediate housing portion 108. The control assembly 107 is a fully-functional mechanical subassembly that can be assembled and tested separately from the rest of the instrument 100 prior to coupling thereto.


Control assembly 107, in cooperation with intermediate housing portion 108, supports a pair of finger-actuated control buttons 124, 126 and a pair rocker devices 128, 130 within a housing 107a. The control buttons 124, 126 are coupled to extension shafts 125, 127 respectively. In particular, control assembly 107 defines an upper aperture 124a for slidably receiving the extension shaft 125, and a lower aperture 126a for slidably receiving the extension shaft 127.


Reference may be made to a commonly-owned U.S. patent application Ser. No. 13/331,047, the entire contents of which are incorporated by reference herein, for a detailed discussion of the construction and operation of the surgical instrument 100.


Referring to FIG. 9, drive assembly 360 of end effector 300 includes a flexible drive shaft 364 having a distal end which is secured to a dynamic drive beam 365, and a proximal engagement section 368. Engagement section 368 includes a stepped portion defining a shoulder 370. A proximal end of engagement section 368 includes diametrically opposed inwardly extending fingers 372. Fingers 372 engage a hollow drive member 374 to fixedly secure drive member 374 to the proximal end of shaft 364. Drive member 374 defines a proximal porthole which receives a connection member of drive tube 246 (FIG. 1) of adapter 200 when end effector 300 is attached to distal coupling 230 of adapter 200.


When drive assembly 360 is advanced distally within tool assembly 304, an upper beam of drive beam 365 moves within a channel defined between anvil plate 312 and anvil cover 310 and a lower beam moves within a channel of the staple cartridge 305 and over the exterior surface of carrier 316 to close tool assembly 304 and fire staples therefrom.


Proximal body portion 302 of end effector 300 includes a sheath or outer tube 301 enclosing an upper housing portion 301a and a lower housing portion 301b. The housing portions 301a and 301b enclose an articulation link 366 having a hooked proximal end 366a which extends from a proximal end of end effector 300. Hooked proximal end 366a of articulation link 366 engages a coupling hook (not shown) of adapter 200 when end effector 300 is secured to distal housing 232 of adapter 200. When drive bar (not shown) of adapter 200 is advanced or retracted as described above, articulation link 366 of end effector 300 is advanced or retracted within end effector 300 to pivot tool assembly 304 in relation to a distal end of proximal body portion 302.


As illustrated in FIG. 9 above, cartridge assembly 308 of tool assembly 304 includes a staple cartridge 305 supportable in carrier 316. Staple cartridge 305 defines a central longitudinal slot 305a, and three linear rows of staple retention slots 305b positioned on each side of longitudinal slot 305a. Each of staple retention slots 305b receives a single staple 307 and a portion of a staple pusher 309. During operation of instrument 100, drive assembly 360 abuts an actuation sled 350 and pushes actuation sled 350 through cartridge 305. As the actuation sled moves through cartridge 305, cam wedges of the actuation sled 350 sequentially engage staple pushers 309 to move staple pushers 309 vertically within staple retention slots 305b and sequentially eject a single staple 307 therefrom for formation against anvil plate 312.


The end effector 300 may also include one or more mechanical lockout mechanisms, such as those described in commonly-owned U.S. Pat. Nos. 5,071,052, 5,397,046, 5413,267, 5,415,335, 5,715,988, 5,718,359, 6,109,500, the entire contents of all of which are incorporated by reference herein.


Another embodiment of the instrument 100 is shown in FIG. 10. The instrument 100 includes the motor 164. The motor 164 may be any electrical motor configured to actuate one or more drives (e.g., rotatable drive connectors 118, 120, 122 of FIG. 6). The motor 164 is coupled to the battery 156, which may be a DC battery (e.g., rechargeable lead-based, nickel-based, lithium-ion based, battery etc.), an AC/DC transformer, or any other power source suitable for providing electrical energy to the motor 164.


The battery 156 and the motor 164 are coupled to a motor driver circuit 404 disposed on the circuit board 154 which controls the operation of the motor 164 including the flow of electrical energy from the battery 156 to the motor 164. The driver circuit 404 includes a plurality of sensors 408a, 408b, . . . 408n configured to measure operational states of the motor 164 and the battery 156. The sensors 408a-n may include voltage sensors, current sensors, temperature sensors, telemetry sensors, optical sensors, and combinations thereof. The sensors 408a-408n may measure voltage, current, and other electrical properties of the electrical energy supplied by the battery 156. The sensors 408a-408n may also measure rotational speed as revolutions per minute (RPM), torque, temperature, current draw, and other operational properties of the motor 164. RPM may be determined by measuring the rotation of the motor 164. Position of various drive shafts (e.g., rotatable drive connectors 118, 120, 122 of FIG. 6) may be determined by using various linear sensors disposed in or in proximity to the shafts or extrapolated from the RPM measurements. In embodiments, torque may be calculated based on the regulated current draw of the motor 164 at a constant RPM. In further embodiments, the driver circuit 404 and/or the controller 406 may measure time and process the above-described values as a function thereof, including integration and/or differentiation, e.g., to determine the change in the measured values and the like.


The driver circuit 404 is also coupled to a controller 406, which may be any suitable logic control circuit adapted to perform the calculations and/or operate according to a set of instructions described in further detail below. The controller 406 may include a central processing unit operably connected to a memory which may include transitory type memory (e.g., RAM) and/or non-transitory type memory (e.g., flash media, disk media, etc.). The controller 406 includes a plurality of inputs and outputs for interfacing with the driver circuit 404. In particular, the controller 406 receives measured sensor signals from the driver circuit 404 regarding operational status of the motor 164 and the battery 156 and, in turn, outputs control signals to the driver circuit 404 to control the operation of the motor 164 based on the sensor readings and specific algorithm instructions, which are discussed in more detail below. The controller 406 is also configured to accept a plurality of user inputs from a user interface (e.g., switches, buttons, touch screen, etc. of the control assembly 107 coupled to the controller 406).


The present disclosure provides for an apparatus and method for controlling the instrument 100 or any other powered surgical instrument, including, but not limited to, linear powered staplers, circular or arcuate powered staplers, graspers, electrosurgical sealing forceps, rotary tissue blending devices, and the like. In particular, torque, RPM, position, and acceleration of drive shafts of the instrument 100 can be correlated to motor characteristics (e.g., current draw). Current drawn by the motor 164 may be used for detecting mechanical limits since the current drawn by the motor 164 changes with the load and speed of the motor 164. Thus, analysis of the amount of change (e.g., rate of change) of current draw allows for distinguishing between different types of load conditions, e.g., load exerted by tissue versus load exerted by a mechanical stop.


During normal operation of the motor 164 the current draw generally does not fall outside a predetermined range (e.g., first range). During clamping and stapling, the load exerted on the motor 164 by the tissue varies within a second range, encompassed by the first range. In particular, as the motor 164 encounters an increased load due to the tissue being clamped by the anvil and cartridge assemblies 306, 308 the current draw increases and is within the second range for a second period of time (e.g., increase in the current draw occurs for a predetermined period of time). If the motor 164 encounters a mechanical limit there is also a corresponding increase in current draw in a relatively short time that is larger than the current draw associated with tissue clamping. In particular, the current draw due to a mechanical stop is within a third range that is higher than the second range for a third period of time. In comparison, startup of the motor 164 draws more current than either clamping/fastening or the mechanical stop and the duration of the increased current draw is the shortest of the two current draws described above.


In embodiments, mechanical stops may be detected by comparing motor current with a predetermined threshold since the current drawn by the motor 164 upon encountering a mechanical stop is usually much higher than the normal operating current. The controller 406 may use the satisfaction of this condition to shut off the motor 164.


This approach presents some challenges when the motor 164 encounters high momentary loads during normal operation (e.g., clamping tissue). The current draw associated with tissue clamping can reach the threshold, thus causing the controller 406 to shut off the motor 164 prematurely. In embodiments, the premature shutoff may be prevented by analyzing normal current draw of the motor 164 and construct a normal motor load profile. The controller 406 may then be programmed to adjust the shutoff threshold in accordance with that profile. This configuration is well-suited to motors 164 having little variation in the load profile. However, large variations can produce false positives if the load profile deviates from the current draw associated with normal use.


Efficiency of the motor 164 and drive mechanism also have an effect in calculating the motor current limit. Since mechanical efficiencies can vary from one instrument to another, each instrument needs to be individually calibrated during assembly. Further, mechanical efficiencies change with wear and tear of the instrument and can also affect performance of the software.


The algorithm according to the present disclosure overcomes the issues of using single-threshold or profile-based algorithms. An advantage of the algorithm according to the present disclosure is that the algorithm utilizes rate of change/current over time rather than comparing amplitude of the motor current to a predetermined threshold. The rate of change of the motor current associated with different loads, e.g., normal load, heavy loads, mechanical stops, load spikes, etc. may be classified into different ranges, in which each range is associated with a specific load. The classification into ranges may then be used to identify distinct loads on the motor 164 and filtering out spikes caused by starting and stopping of the motor 164. Since the identification of the mechanical loads is based on the rate of change in motor current rather than its amplitude, deviation from the load profiles do not affect load identification. In addition, mechanical efficiencies do not affect load identification based on rate of change in motor current. Less efficient instruments draw more current to attain the same speed, however, the slopes (e.g., rate of change in current draw) for reaching those speeds remains similar to those of more efficient systems. This eliminates the need for load profiling and calibration operation during assembly of the instrument 100.


Another advantage of the algorithm according to the present disclosure is the low computational overhead. The algorithm relies on calculating the rate of change of the motor current and as such can be determined by taking the difference between two values, allowing for implementation of the algorithm in an 8-bit microcontroller.


The change in motor current can be measured by sampling current periodically. In embodiments, the sampling rate may be from about 100 per second to about 10,000 per second, in embodiments from about 500 per second to about 1,000 per second. The samples may then be used by the controller 406 to calculate the change in the motor current (e.g., current draw). The controller 406 may then use the change in motor current to determine the operating condition of the instrument 100 and take appropriate action.


The present disclosure also provides a feedback system and method for controlling the instrument 100 based on external operating conditions such as firing difficulty encountered by the instrument 100 due to tissue thickness and/or mechanical stop (e.g., the drive beam 365 reaching the distal end of the channel defined in the anvil plate 312 and the staple cartridge 305. In addition, the present disclosure provides for modeling of different usages of the instrument 100 in response to the external operating conditions (e.g., specific failures) to derive internal system feedback. The sensor information from the sensors 408a-n is used by the controller 406 to alter operating characteristics of the instrument 100 and/or notify users of specific operational conditions. In embodiments, the controller 406 controls (e.g., limits) the current supplied to the motor 164.


The controller 406 includes a computer-readable memory 406a and/or non-transitory medium for storing software instructions (e.g., algorithm) for detecting mechanical limits of the instrument 100 based on the measured current draw. As used herein, the term “mechanical limit” denotes any of the electromechanical components reaching end-of-travel positions including, but not limited to, e.g., the drive beam 365 reaching the distal end of the channel defined in the anvil plate 312 and the staple cartridge 305, actuation of mechanical safety lockout mechanisms preventing travel of the shaft 364, articulation link 366 reaching articulation limits of the end effector 300, and the like.


The change in motor current associated with the onset of certain load conditions (e.g., tissue clamping or mechanical limits) falls within predefined ranges and persists for a certain duration. These conditions are used by the algorithm to identify operating properties of the motor 164 and react accordingly in response thereto.


With reference to FIG. 11, the memory 406a stores a plurality of current draw values. The memory 406a includes look-up table 500 or any other suitable data structure having values “I-V.” The first value I and the fifth value “V” define a first range encompassing a stable current draw signal indicative of normal (e.g., load-bearing) operation of the motor 164. The second and third values “II” and “III” define a second range corresponding to the current draw associated with current draw of the motor 164 during tissue clamping and fourth and fifth values “IV” and “V” defining a third range corresponding to the current draw associated with a mechanical stop. In embodiments, the first value “I” may be the same as the second value “II.”


The controller 406 also includes a condition-of-interest counter which counts the number of samples during which the slope (e.g., rate of change) of the motor current lies within the desired range (e.g., either first, second or third ranges). The controller 406 also includes a signal stability counter, which counts the number of samples for which the slope lies within the second range. The controller 406 determines if the measured rate of change current draw signal is stable using the values of the table 500. The signal is considered to be unstable if a predetermined number of current draw samples are outside the first range and stable if a predetermined number of samples are within the second range.



FIG. 12 shows a method according to the present disclosure for determining if the motor 164 encounters a mechanical stop. The method may be implemented as software instructions (e.g., algorithm) stored in the controller 406 as described above. Initially, the controller 406 calculates a moving average of the measured motor current (e.g., current draw). As used herein, the term “moving average” denotes an average of a predetermined subset of samples that is updated every time a new sample is obtained. The moving average may include from about 2 plurality of samples to about 256 plurality of samples, and in embodiments, from about plurality of samples 16 about plurality of samples 64, depending on the sampling rate described above. The controller 406 stores the first moving average and calculates the second moving average for the subsequent sample set. The controller 406 then determines the difference between the moving averages to calculate the sample-to-sample change.


As shown in FIGS. 12-13, the moving average of the samples may be graphed as plots 700, 800, 900, with the sample-to-sample change being represented as the slope of the plots 700, 800, 900. The plots 700, 800, 900 may be generated and outputted on a display allowing the user to view the current draw of the motor 164. In embodiments, the plots 700, 800, 900 may be stored in the memory 406a as a series of values, without reproducing the sample values as a plot.


The change in the monitored motor current, also defined as the slope is used to differentiate between different types of loads encountered by motor 164. The controller 406 initially determines if the signal is stable by determining whether the calculated slope/change is outside the first range (e.g., the slope is larger than fifth value “V” or less than first value “I”). If the slope lies outside the first range for a predefined number of samples, the controller 406 initializes or resets the condition-of-interest and signal stability counters by setting them to zero, 0. In addition, the controller 406 also sets the signal status as “unstable.”


With reference to FIGS. 14 and 15, the samples below first value “I,” as shown in FIG. 14, and above the fifth value “V,” as shown in FIG. 15, are filtered out since they represent abnormal negative and positive spikes in current draw. These spikes may be caused by starting and stopping of the motor 164 and may result false positives in threshold-based decision making algorithms.


After determining if the slope is outside the first range, the controller 406 determines if the slope is within the second range (value II≤slope≤value III). If so, the stability counter is incremented. The controller 406 checks if the stability counter has reached a predetermined threshold before changing the signal status to “stable.” This ensures that the sample has been within the second range for a sufficient period of time. Any deviation, e.g., the slope being outside the first range, resets the condition-of-interest and signal stability counters and sets the signal status as “unstable” as described above.


With reference to FIGS. 13-15, the signal is considered to be stable if the slope is within the second range, irrelevant of the actual amplitude of the motor current samples. Thus, the higher amplitude of the samples within the second range of FIG. 15 and lower amplitude of the samples within the second range of FIGS. 13 and 14 is treated similarly by the algorithm of the present disclosure as the attribute of interest is the rate of change of slope of the motor current samples.


The controller 406 also determines if the sample is within the third range. For each sample within the third range, while the signal is deemed stable, the condition-of-interest counter is incremented. Every time the sample falls below second value “II,” the condition-of-interest counter is decremented. The condition-of-interest counter is used to identify a mechanical stop, as described in further detail below. If the condition-of-interest counter is above a predetermined threshold, then the controller 406 determines that a mechanical stop has been reached. With reference to FIG. 13, a plurality of samples have a slope that falls within the third range, this increments the condition-of-interest counter and upon reaching the predetermined count triggers the indication that the mechanical stop has been reached. Once the controller 406 determines that the mechanical limit has been reached the supply of current to the motor 164 may be terminated to prevent further operation of the instrument 100 and/or the instrument 100 may issue an alarm.



FIG. 16 shows a method according another embodiment of to the present disclosure for determining if the motor 164 encounters a mechanical stop.


The controller 406 includes the stability and condition-of-interest counters, as described above. The controller 406 further includes a positive spike counter and a negative spike counter. These counters maintain a number of times a current (e.g., slope) has spiked outside the first range. More specifically, the positive spike counter is incremented when the motor current is above the value “V” and the negative spike counter is incremented when the motor current is below the value “I.” The controller 406 determines if the measured rate of change current draw signal is stable using the values of the table 500. The signal is considered to be unstable if a predetermined number of current draw samples are outside the first range (e.g., is the number of positive and negative spikes is above a predetermined positive and negative spike threshold) and stable if a predetermined number of samples are within the second range.


The method of FIG. 16 may also be implemented as software instructions (e.g., algorithm) stored in the controller 406 as described above. Initially, the controller 406 calculates a moving average of the measured motor current (e.g., current draw). As used herein, the term “moving average” denotes an average of a predetermined subset of samples that is updated every time a new sample is obtained. The moving average may include from about 2 samples to about 256 samples, and in embodiments, from about 16 to about 64 samples, depending on the sampling rate described above. The controller 406 stores the first moving average and calculates the second moving average for the subsequent sample set. The controller 406 then determines the difference between the moving averages to calculate the sample-to-sample change (e.g., slope).


The change in the monitored motor current, also defined as the slope, is used to differentiate between different types of loads encountered by motor 164. The controller 406 initially determines if the slope is larger than fifth value “V” and updated the previous moving average to the presently calculated moving average. If the slope is above the fifth value “V,” the positive spike counter is incremented while the negative spike counter is decremented. In addition, the controller 406 verifies if the positive spike counter is above a predetermined positive spike counter threshold. If so, the controller 406 initializes or resets the condition-of-interest and signal stability counters by setting them to zero, 0. In addition, the controller 406 also sets the signal status as “unstable.” If the positive spike counter is below the predetermined positive spike counter threshold, the stability counter is decremented.


After determining if the slope is above the fifth value “V,” the controller 406 determines if the sample falls below second value “II,” the condition-of-interest counter is decremented.


The controller 406 also determines if the slope is smaller than the first value “I” and updated the previous moving average to the presently calculated moving average. If the slope is above the first value “I,” the negative spike counter is incremented while the positive spike counter is decremented. In addition, the controller 406 verifies if the negative spike counter is above a predetermined negative spike counter threshold. If so, the controller 406 initializes or resets the condition-of-interest and signal stability counters by setting them to zero, 0. In addition, the controller 406 also sets the signal status as “unstable.” If the negative spike counter is below the predetermined negative spike counter threshold, the stability counter is decremented.


With reference to FIGS. 14 and 15, the samples below first value “I,” as shown in FIG. 14, and above the fifth value “V,” as shown in FIG. 15, are filtered out since they represent abnormal negative and positive spikes in current draw. These spikes may be caused by starting and stopping of the motor 164 and may result false positives in threshold-based decision making algorithms.


The controller 406 also determines if the slope is within the second range (e.g., value “II”≤slope≤value “III”). If so, the stability counter is incremented. The controller 406 also checks if the stability counter has reached a predetermined threshold before changing the signal status to “stable.” This ensures that the sample has been within the second range for a sufficient period of time. In addition, the controller 406 initializes or resets the positive and negative spike counters by setting them to zero, 0. Regardless whether the stability counter is below or above the predetermined threshold, the previous moving average is updated to the presently calculated moving average. Any deviation, e.g., the slope being outside the first range, also resets the condition-of-interest and signal stability counters and sets the signal status as “unstable” as described above.


The controller 406 also determines if the sample is within the third range. For each sample within the third range, while the signal is deemed stable, the condition-of-interest counter is incremented. The condition-of-interest counter is used to identify a mechanical stop, as described in further detail below. If the condition-of-interest counter is above a predetermined threshold, then the controller 406 determines that a mechanical stop has been reached. With reference to FIG. 13, a plurality of samples have a slope that falls within the third range, this increments the condition-of-interest counter and upon reaching the predetermined count triggers the indication that the mechanical stop has been reached. Once the controller 406 determines that the mechanical limit has been reached the supply of current to the motor 164 may be terminated to prevent further operation of the instrument 100 and/or the instrument 100 may issue an alarm.


In addition to basic feedback about device performance the present disclosure also provides a method for powered devices to detect and discern other external factors, e.g., thicker tissue, which previously were difficult to detect. As a result, improved cutoffs and values for limits can be implemented, greatly improving the safety of powered devices in use. Using the feedback mechanisms discussed above, users may make intelligent decisions about what settings and techniques should be used when operating the instrument 100. This intelligence can range from choosing a different reload to fire with a linear stapler, deciding to fire at a different articulation angle, to choosing to use a completely different surgical technique.


It should be understood that the foregoing description is only illustrative of the present disclosure. Various alternatives and modifications can be devised by those skilled in the art without departing from the disclosure. Accordingly, the present disclosure is intended to embrace all such alternatives, modifications and variances. The embodiments described with reference to the attached drawing figures are presented only to demonstrate certain examples of the disclosure. Other elements, steps, methods and techniques that are insubstantially different from those described above and/or in the appended claims are also intended to be within the scope of the disclosure.

Claims
  • 1. A surgical instrument, comprising: a handle assembly;a jaw assembly comprising a staple cartridge containing a plurality of staples and an anvil to form the plurality of staples upon firing;a drive assembly at least partially located within the handle assembly and connected to the jaw assembly and a lockout mechanism;a motor disposed within the handle assembly and operatively coupled to the drive assembly; anda controller operatively coupled to the motor, the controller configured to: measure a plurality of current draw samples of a current draw of the motor;determine a rate of change of the current draw;store a first stability counter corresponding to current draw samples whose rate of change is within a first range of rate of change values; andterminate a supply of electrical current to the motor based on the rate of change of the current draw being within the first range of rate of change values, and the first stability counter being above a predetermined stability threshold,wherein the first range of rate of change values corresponds to a current draw indicative of a mechanical limit of at least one of the jaw assembly, the drive assembly, or the motor.
  • 2. The surgical instrument according to claim 1, wherein the controller is further configured to determine whether the current draw is stable based on the rate of change of the current draw being within a second range of rate of change values.
  • 3. The surgical instrument according to claim 2, wherein the controller is further configured to determine whether the current draw is unstable based on the rate of change of the current draw being within a third range of rate of change values.
  • 4. The surgical instrument according to claim 3, wherein the controller is further configured to store a second stability counter of current draw samples within the second range.
  • 5. The surgical instrument according to claim 4, wherein the controller determines whether the current draw is stable when the second stability counter is above a predetermined stability threshold.
  • 6. The surgical instrument according to claim 5, wherein the first range is within the second range and the third range extends higher than the second range.
  • 7. The surgical instrument according to claim 5, wherein the controller is further configured to store an event counter of current draw samples within the third range.
  • 8. A surgical instrument, comprising: a handle assembly;a jaw assembly comprising a staple cartridge containing a plurality of staples and an anvil to form the plurality of staples upon firing;a drive assembly at least partially located within the handle assembly and connected to the jaw assembly and a lockout mechanism;a motor disposed within the handle assembly and operatively coupled to the drive assembly; anda controller operatively coupled to the motor, the controller configured to: measure a plurality of current draw samples of a current draw of the motor to determine a rate of change of the current draw,store a first stability counter of current draw samples measured when the rate of change of the current draw is within a first range of rate of change values, anddetermine whether the motor has reached a mechanical limit based on the rate of change of the current draw being within a first range of rate of change values indicative of the mechanical limit, and the first stability counter being above a predetermined stability threshold.
  • 9. The surgical instrument according to claim 8, wherein the controller is further configured to determine whether the current draw is stable based on the rate of change of the current draw being within a second range of rate of change values.
  • 10. The surgical instrument according to claim 9, wherein the controller is further configured to determine whether the current draw is unstable based on the rate of change of the current draw being within a third range of rate of change values.
  • 11. The surgical instrument according to claim 10, wherein the controller is further configured to store a second stability counter of current draw samples within the second range.
  • 12. The surgical instrument according to claim 11, wherein the controller determines whether the current draw is stable when the second stability counter is above a predetermined stability threshold.
  • 13. The surgical instrument according to claim 12, wherein the first range is within the second range and the third range is higher than the second range.
  • 14. The surgical instrument according to claim 12, wherein the controller is further configured to store an event counter of current draw samples within the third range.
CROSS-REFERENCE TO RELATED APPLICATION

The present application claims the benefit of and priority to a U.S. Provisional Patent Application Ser. No. 61/879,445, filed on Sep. 18, 2013, the entire contents of which are incorporated by reference herein.

US Referenced Citations (407)
Number Name Date Kind
2245994 McWane Jun 1941 A
2777340 Hettwer et al. Jan 1957 A
2957353 Babacz Oct 1960 A
3111328 Di Rito et al. Nov 1963 A
3695058 Keith, Jr. Oct 1972 A
3734515 Dudek May 1973 A
3759336 Marcovitz et al. Sep 1973 A
4162399 Hudson Jul 1979 A
4606343 Conta et al. Aug 1986 A
4705038 Sjostrom et al. Nov 1987 A
4722685 de Estrada et al. Feb 1988 A
4823807 Russell et al. Apr 1989 A
4874181 Hsu Oct 1989 A
5129118 Walmesley Jul 1992 A
5129570 Schulze et al. Jul 1992 A
5152744 Krause et al. Oct 1992 A
5301061 Nakada et al. Apr 1994 A
5312023 Green et al. May 1994 A
5326013 Green et al. Jul 1994 A
5350355 Sklar Sep 1994 A
5383874 Jackson et al. Jan 1995 A
5383880 Hooven Jan 1995 A
5389098 Tsuruta et al. Feb 1995 A
5395033 Byrne et al. Mar 1995 A
5400267 Denen et al. Mar 1995 A
5411508 Bessler et al. May 1995 A
5413267 Solyntjes et al. May 1995 A
5427087 Ito et al. Jun 1995 A
5467911 Tsuruta et al. Nov 1995 A
5476379 Disel Dec 1995 A
5487499 Sorrentino et al. Jan 1996 A
5518163 Hooven May 1996 A
5518164 Hooven May 1996 A
5526822 Burbank et al. Jun 1996 A
5529235 Boiarski et al. Jun 1996 A
5535934 Boiarski et al. Jul 1996 A
5535937 Boiarski et al. Jul 1996 A
5540375 Bolanos et al. Jul 1996 A
5540706 Aust et al. Jul 1996 A
5542594 McKean et al. Aug 1996 A
5549637 Crainich Aug 1996 A
5553675 Pitzen et al. Sep 1996 A
5562239 Boiarski et al. Oct 1996 A
5564615 Bishop et al. Oct 1996 A
5609560 Ichikawa et al. Mar 1997 A
5632432 Schulze et al. May 1997 A
5647526 Green et al. Jul 1997 A
5653374 Young et al. Aug 1997 A
5658300 Bito et al. Aug 1997 A
5667517 Hooven Sep 1997 A
5693042 Boiarski et al. Dec 1997 A
5704534 Huitema et al. Jan 1998 A
5713505 Huitema Feb 1998 A
5762603 Thompson Jun 1998 A
5779130 Alesi et al. Jul 1998 A
5782396 Mastri et al. Jul 1998 A
5782397 Koukline Jul 1998 A
5797536 Smith et al. Aug 1998 A
5820009 Melling et al. Oct 1998 A
5863159 Lasko Jan 1999 A
5865361 Milliman et al. Feb 1999 A
5908427 McKean et al. Jun 1999 A
5954259 Viola et al. Sep 1999 A
5964774 McKean et al. Oct 1999 A
5993454 Longo Nov 1999 A
6010054 Johnson et al. Jan 2000 A
6017354 Culp et al. Jan 2000 A
6032849 Mastri et al. Mar 2000 A
6045560 McKean et al. Apr 2000 A
6090123 Culp et al. Jul 2000 A
6126651 Mayer Oct 2000 A
6129547 Cise et al. Oct 2000 A
6165169 Panescu et al. Dec 2000 A
6239732 Cusey May 2001 B1
6241139 Milliman et al. Jun 2001 B1
6264086 McGuckin, Jr. Jul 2001 B1
6264087 Whitman Jul 2001 B1
6302311 Adams et al. Oct 2001 B1
6315184 Whitman Nov 2001 B1
6321855 Barnes Nov 2001 B1
6329778 Culp et al. Dec 2001 B1
6343731 Adams et al. Feb 2002 B1
6348061 Whitman Feb 2002 B1
6368324 Dinger et al. Apr 2002 B1
6371909 Hoeg et al. Apr 2002 B1
6434507 Clayton et al. Aug 2002 B1
6443973 Whitman Sep 2002 B1
6461372 Jensen et al. Oct 2002 B1
6488197 Whitman Dec 2002 B1
6491201 Whitman Dec 2002 B1
6533157 Whitman Mar 2003 B1
6537280 Dinger et al. Mar 2003 B2
6610066 Dinger et al. Aug 2003 B2
6611793 Burnside et al. Aug 2003 B1
6645218 Cassidy et al. Nov 2003 B1
6654999 Stoddard et al. Dec 2003 B2
6698643 Whitman Mar 2004 B2
6699177 Wang et al. Mar 2004 B1
6716233 Whitman Apr 2004 B1
6743240 Smith et al. Jun 2004 B2
6783533 Green et al. Aug 2004 B2
6792390 Burnside et al. Sep 2004 B1
6793652 Whitman et al. Sep 2004 B1
6817508 Racenet et al. Nov 2004 B1
6830174 Hillstead et al. Dec 2004 B2
6846308 Whitman et al. Jan 2005 B2
6846309 Whitman et al. Jan 2005 B2
6849071 Whitman et al. Feb 2005 B2
6899538 Matoba May 2005 B2
6905057 Swayze et al. Jun 2005 B2
6959852 Shelton, IV et al. Nov 2005 B2
6964363 Wales et al. Nov 2005 B2
6981628 Wales Jan 2006 B2
6981941 Whitman et al. Jan 2006 B2
6986451 Mastri et al. Jan 2006 B1
6988649 Shelton, IV et al. Jan 2006 B2
7032798 Whitman et al. Apr 2006 B2
RE39152 Aust et al. Jun 2006 E
7055731 Shelton, IV et al. Jun 2006 B2
7059508 Shelton, IV et al. Jun 2006 B2
7077856 Whitman Jul 2006 B2
7111769 Wales et al. Sep 2006 B2
7122029 Koop et al. Oct 2006 B2
7140528 Shelton, IV Nov 2006 B2
7143923 Shelton, IV et al. Dec 2006 B2
7143925 Shelton, IV et al. Dec 2006 B2
7143926 Shelton, IV et al. Dec 2006 B2
7147138 Shelton, IV Dec 2006 B2
7172104 Scirica et al. Feb 2007 B2
7225964 Mastri et al. Jun 2007 B2
7238021 Johnson Jul 2007 B1
7246734 Shelton, IV Jul 2007 B2
7328828 Ortiz et al. Feb 2008 B2
7364061 Swayze et al. Apr 2008 B2
7380695 Doll et al. Jun 2008 B2
7380696 Shelton, IV et al. Jun 2008 B2
7404508 Smith et al. Jul 2008 B2
7407078 Shelton, IV et al. Aug 2008 B2
7416101 Shelton, IV et al. Aug 2008 B2
7419080 Smith et al. Sep 2008 B2
7422139 Shelton, IV et al. Sep 2008 B2
7431189 Shelton, IV et al. Oct 2008 B2
7441684 Shelton, IV et al. Oct 2008 B2
7448525 Shelton, IV et al. Nov 2008 B2
7464846 Shelton, IV et al. Dec 2008 B2
7464847 Viola et al. Dec 2008 B2
7464849 Shelton, IV et al. Dec 2008 B2
7481347 Roy Jan 2009 B2
7481824 Boudreaux et al. Jan 2009 B2
7487899 Shelton, IV et al. Feb 2009 B2
7549564 Boudreaux Jun 2009 B2
7565993 Milliman et al. Jul 2009 B2
7568603 Shelton, IV et al. Aug 2009 B2
7575144 Ortiz et al. Aug 2009 B2
7588175 Timm et al. Sep 2009 B2
7588176 Timm et al. Sep 2009 B2
7637409 Marczyk Dec 2009 B2
7641093 Doll et al. Jan 2010 B2
7644848 Swayze et al. Jan 2010 B2
7670334 Hueil et al. Mar 2010 B2
7673780 Shelton, IV et al. Mar 2010 B2
7699835 Lee et al. Apr 2010 B2
7721931 Shelton, IV et al. May 2010 B2
7738971 Swayze et al. Jun 2010 B2
7740159 Shelton, IV et al. Jun 2010 B2
7743960 Whitman et al. Jun 2010 B2
7758613 Whitman Jul 2010 B2
7766210 Shelton, IV et al. Aug 2010 B2
7770773 Whitman et al. Aug 2010 B2
7770775 Shelton, IV et al. Aug 2010 B2
7793812 Moore et al. Sep 2010 B2
7799039 Shelton, IV et al. Sep 2010 B2
7802712 Milliman et al. Sep 2010 B2
7803151 Whitman Sep 2010 B2
7822458 Webster, III et al. Oct 2010 B2
7845534 Viola et al. Dec 2010 B2
7845537 Shelton, IV et al. Dec 2010 B2
7857185 Swayze et al. Dec 2010 B2
7870989 Viola et al. Jan 2011 B2
7905897 Whitman et al. Mar 2011 B2
7918230 Whitman et al. Apr 2011 B2
7922061 Shelton, IV et al. Apr 2011 B2
7922719 Ralph et al. Apr 2011 B2
7947034 Whitman May 2011 B2
7951071 Whitman et al. May 2011 B2
7954682 Giordano et al. Jun 2011 B2
7959051 Smith et al. Jun 2011 B2
7963433 Whitman et al. Jun 2011 B2
7967178 Scirica et al. Jun 2011 B2
7967179 Olson et al. Jun 2011 B2
7992758 Whitman et al. Aug 2011 B2
8016178 Olson et al. Sep 2011 B2
8016855 Whitman et al. Sep 2011 B2
8020743 Shelton, IV Sep 2011 B2
8025199 Whitman et al. Sep 2011 B2
8035487 Malackowski Oct 2011 B2
8052024 Viola et al. Nov 2011 B2
8056787 Boudreaux et al. Nov 2011 B2
8114118 Knodel et al. Feb 2012 B2
8132705 Viola et al. Mar 2012 B2
8152516 Harvey et al. Apr 2012 B2
8157150 Viola et al. Apr 2012 B2
8157151 Ingmanson et al. Apr 2012 B2
8182494 Yencho et al. May 2012 B1
8186555 Shelton, IV et al. May 2012 B2
8186587 Zmood et al. May 2012 B2
8220367 Hsu Jul 2012 B2
8235273 Olson et al. Aug 2012 B2
8241322 Whitman et al. Aug 2012 B2
8272554 Whitman et al. Sep 2012 B2
8292150 Bryant Oct 2012 B2
8292888 Whitman Oct 2012 B2
8303581 Arts et al. Nov 2012 B2
8342379 Whitman et al. Jan 2013 B2
8348855 Hillely et al. Jan 2013 B2
8353440 Whitman et al. Jan 2013 B2
8357144 Whitman et al. Jan 2013 B2
8365633 Simaan et al. Feb 2013 B2
8365972 Aranyi et al. Feb 2013 B2
8371492 Aranyi et al. Feb 2013 B2
8372057 Cude et al. Feb 2013 B2
8391957 Carlson et al. Mar 2013 B2
8424739 Racenet et al. Apr 2013 B2
8454585 Whitman Jun 2013 B2
8505802 Viola et al. Aug 2013 B2
8517241 Nicholas et al. Aug 2013 B2
8551076 Duval et al. Oct 2013 B2
8561871 Rajappa et al. Oct 2013 B2
8623000 Humayun et al. Jan 2014 B2
8632463 Drinan et al. Jan 2014 B2
8647258 Aranyi et al. Feb 2014 B2
8657174 Yates et al. Feb 2014 B2
8657177 Scirica et al. Feb 2014 B2
8672206 Aranyi et al. Mar 2014 B2
8696552 Whitman Apr 2014 B2
8708213 Shelton, IV et al. Apr 2014 B2
8752749 Moore et al. Jun 2014 B2
8758391 Swayze et al. Jun 2014 B2
8806973 Ross et al. Aug 2014 B2
8851355 Aranyi et al. Oct 2014 B2
8858571 Shelton, IV et al. Oct 2014 B2
8875972 Weisenburgh, II et al. Nov 2014 B2
8893946 Boudreaux et al. Nov 2014 B2
8899462 Kostrzewski et al. Dec 2014 B2
8939344 Olson et al. Jan 2015 B2
8960519 Whitman et al. Feb 2015 B2
8961396 Azarbarzin et al. Feb 2015 B2
8967443 McCuen Mar 2015 B2
8968276 Zemlok et al. Mar 2015 B2
8968337 Whitfield et al. Mar 2015 B2
8992422 Spivey et al. Mar 2015 B2
9064653 Prest et al. Jun 2015 B2
9113875 Viola et al. Aug 2015 B2
9216013 Scirica et al. Dec 2015 B2
9282961 Whitman et al. Mar 2016 B2
9282963 Bryant Mar 2016 B2
9295522 Kostrzewski Mar 2016 B2
9307986 Hall et al. Apr 2016 B2
20010031975 Whitman et al. Oct 2001 A1
20020049454 Whitman et al. Apr 2002 A1
20020165541 Whitman Nov 2002 A1
20030038938 Jung et al. Feb 2003 A1
20030165794 Matoba Sep 2003 A1
20040111012 Whitman Jun 2004 A1
20040133189 Sakurai Jul 2004 A1
20040176751 Weitzner et al. Sep 2004 A1
20040193146 Lee et al. Sep 2004 A1
20050131442 Yachia et al. Jun 2005 A1
20060142656 Malackowski et al. Jun 2006 A1
20060142740 Sherman et al. Jun 2006 A1
20060142744 Boutoussov Jun 2006 A1
20060259073 Miyamoto et al. Nov 2006 A1
20060278680 Viola et al. Dec 2006 A1
20070023476 Whitman et al. Feb 2007 A1
20070023477 Whitman et al. Feb 2007 A1
20070029363 Popov Feb 2007 A1
20070049435 Jinno et al. Mar 2007 A1
20070055219 Whitman et al. Mar 2007 A1
20070084897 Shelton et al. Apr 2007 A1
20070102472 Shelton May 2007 A1
20070152014 Gillum et al. Jul 2007 A1
20070175947 Ortiz et al. Aug 2007 A1
20070175949 Shelton et al. Aug 2007 A1
20070175950 Shelton et al. Aug 2007 A1
20070175951 Shelton et al. Aug 2007 A1
20070175955 Shelton et al. Aug 2007 A1
20070175961 Shelton et al. Aug 2007 A1
20080029570 Shelton et al. Feb 2008 A1
20080029573 Shelton et al. Feb 2008 A1
20080029574 Shelton et al. Feb 2008 A1
20080029575 Shelton et al. Feb 2008 A1
20080058801 Taylor et al. Mar 2008 A1
20080109012 Falco et al. May 2008 A1
20080110958 McKenna et al. May 2008 A1
20080167670 Shelton et al. Jul 2008 A1
20080167736 Swayze et al. Jul 2008 A1
20080185419 Smith et al. Aug 2008 A1
20080188841 Tomasello et al. Aug 2008 A1
20080197167 Viola et al. Aug 2008 A1
20080208195 Shores et al. Aug 2008 A1
20080237296 Boudreaux et al. Oct 2008 A1
20080251561 Eades et al. Oct 2008 A1
20080255413 Zemlok et al. Oct 2008 A1
20080255607 Zemlok Oct 2008 A1
20080262654 Omori et al. Oct 2008 A1
20080308603 Shelton et al. Dec 2008 A1
20090090763 Zemlok et al. Apr 2009 A1
20090099876 Whitman Apr 2009 A1
20090138006 Bales et al. May 2009 A1
20090171147 Lee et al. Jul 2009 A1
20090182193 Whitman et al. Jul 2009 A1
20090209990 Yates et al. Aug 2009 A1
20090254094 Knapp et al. Oct 2009 A1
20100069942 Shelton, IV Mar 2010 A1
20100193568 Scheib et al. Aug 2010 A1
20100211053 Ross et al. Aug 2010 A1
20100225073 Porter et al. Sep 2010 A1
20110006101 Hall et al. Jan 2011 A1
20110017801 Zemlok Jan 2011 A1
20110071508 Duval et al. Mar 2011 A1
20110077673 Grubac et al. Mar 2011 A1
20110121049 Malinouskas et al. May 2011 A1
20110125138 Malinouskas et al. May 2011 A1
20110139851 McCuen Jun 2011 A1
20110155783 Rajappa et al. Jun 2011 A1
20110155786 Shelton, IV Jun 2011 A1
20110172648 Jeong Jul 2011 A1
20110174099 Ross et al. Jul 2011 A1
20110204119 McCuen Aug 2011 A1
20110218522 Whitman Sep 2011 A1
20110253765 Nicholas et al. Oct 2011 A1
20110276057 Conlon et al. Nov 2011 A1
20110290854 Timm et al. Dec 2011 A1
20110290855 Moore et al. Dec 2011 A1
20110295242 Spivey et al. Dec 2011 A1
20110295269 Swensgard et al. Dec 2011 A1
20120000962 Racenet et al. Jan 2012 A1
20120074199 Olson et al. Mar 2012 A1
20120089131 Zemlok et al. Apr 2012 A1
20120104071 Bryant May 2012 A1
20120116368 Viola May 2012 A1
20120143002 Aranyi et al. Jun 2012 A1
20120172924 Allen, IV Jul 2012 A1
20120223121 Viola et al. Sep 2012 A1
20120245428 Smith et al. Sep 2012 A1
20120253329 Zemlok et al. Oct 2012 A1
20120310220 Malkowski et al. Dec 2012 A1
20120323226 Chowaniec et al. Dec 2012 A1
20120330285 Hartoumbekis et al. Dec 2012 A1
20130018361 Bryant Jan 2013 A1
20130093149 Saur et al. Apr 2013 A1
20130098966 Kostrzewski et al. Apr 2013 A1
20130098968 Aranyi et al. Apr 2013 A1
20130098969 Scirica et al. Apr 2013 A1
20130181035 Milliman Jul 2013 A1
20130184704 Beardsley et al. Jul 2013 A1
20130214025 Zemlok et al. Aug 2013 A1
20130240596 Whitman Sep 2013 A1
20130274722 Kostrzewski et al. Oct 2013 A1
20130282052 Aranyi et al. Oct 2013 A1
20130292451 Viola et al. Nov 2013 A1
20130313304 Shelton, IV et al. Nov 2013 A1
20130317486 Nicholas et al. Nov 2013 A1
20130319706 Nicholas et al. Dec 2013 A1
20130324978 Nicholas et al. Dec 2013 A1
20130324979 Nicholas et al. Dec 2013 A1
20130334281 Williams Dec 2013 A1
20140012236 Williams et al. Jan 2014 A1
20140012237 Pribanic et al. Jan 2014 A1
20140012289 Snow et al. Jan 2014 A1
20140025046 Williams et al. Jan 2014 A1
20140110455 Ingmanson et al. Apr 2014 A1
20140144970 Aranyi et al. May 2014 A1
20140207125 Applegate et al. Jul 2014 A1
20140207182 Zergiebel et al. Jul 2014 A1
20140207185 Goble et al. Jul 2014 A1
20140236173 Scirica et al. Aug 2014 A1
20140236174 Williams et al. Aug 2014 A1
20140276932 Williams et al. Sep 2014 A1
20140299647 Scirica et al. Oct 2014 A1
20140303668 Nicholas et al. Oct 2014 A1
20140358129 Zergiebel et al. Dec 2014 A1
20140361068 Aranyi et al. Dec 2014 A1
20140373652 Zergiebel et al. Dec 2014 A1
20150048144 Whitman Feb 2015 A1
20150076205 Zergiebel Mar 2015 A1
20150080912 Sapre Mar 2015 A1
20150157321 Zergiebel et al. Jun 2015 A1
20150164502 Richard et al. Jun 2015 A1
20150272577 Zemlok et al. Oct 2015 A1
20150297199 Nicholas et al. Oct 2015 A1
20150303996 Calderoni Oct 2015 A1
20150320420 Penna et al. Nov 2015 A1
20150327850 Kostrzewski Nov 2015 A1
20150342601 Williams et al. Dec 2015 A1
20150342603 Zergiebel et al. Dec 2015 A1
20150374366 Zergiebel et al. Dec 2015 A1
20150374370 Zergiebel et al. Dec 2015 A1
20150374371 Richard et al. Dec 2015 A1
20150374372 Zergiebel et al. Dec 2015 A1
20150374449 Chowaniec et al. Dec 2015 A1
20150380187 Zergiebel et al. Dec 2015 A1
20160095585 Zergiebel et al. Apr 2016 A1
20160095596 Scirica et al. Apr 2016 A1
20160106406 Cabrera et al. Apr 2016 A1
20160113648 Zergiebel et al. Apr 2016 A1
20160113649 Zergiebel et al. Apr 2016 A1
Foreign Referenced Citations (81)
Number Date Country
2008229795 Apr 2009 AU
2451558 Jan 2003 CA
101234033 Aug 2008 CN
101856251 Oct 2010 CN
102028509 Apr 2011 CN
102247182 Nov 2011 CN
102008053842 May 2010 DE
0634144 Jan 1995 EP
0648476 Apr 1995 EP
0686374 Dec 1995 EP
0705571 Apr 1996 EP
1690502 Aug 2006 EP
1723913 Nov 2006 EP
1736112 Dec 2006 EP
1759652 Mar 2007 EP
1769754 Apr 2007 EP
1772105 Apr 2007 EP
1 813 203 Aug 2007 EP
1813199 Aug 2007 EP
1813211 Aug 2007 EP
1908412 Apr 2008 EP
1917929 May 2008 EP
1943954 Jul 2008 EP
1943956 Jul 2008 EP
1943958 Jul 2008 EP
1943976 Jul 2008 EP
1952769 Aug 2008 EP
2005898 Dec 2008 EP
2027819 Feb 2009 EP
2044890 Apr 2009 EP
2055243 May 2009 EP
2090247 Aug 2009 EP
2098170 Sep 2009 EP
2100561 Sep 2009 EP
2100562 Sep 2009 EP
2165664 Mar 2010 EP
2236098 Oct 2010 EP
2245994 Nov 2010 EP
2263568 Dec 2010 EP
2272443 Jan 2011 EP
2316345 May 2011 EP
2324776 May 2011 EP
2329773 Jun 2011 EP
2333509 Jun 2011 EP
2377472 Oct 2011 EP
2462878 Jun 2012 EP
2462880 Jun 2012 EP
2491872 Aug 2012 EP
2586382 May 2013 EP
2606834 Jun 2013 EP
2668910 Dec 2013 EP
2676615 Dec 2013 EP
2815705 Dec 2014 EP
2333509 Feb 2010 ES
2861574 May 2005 FR
08-038488 Feb 1996 JP
2005-125075 May 2005 JP
20120022521 Mar 2012 KR
9915086 Apr 1999 WO
2000072760 Dec 2000 WO
2000072765 Dec 2000 WO
2003000138 Jan 2003 WO
2003026511 Apr 2003 WO
2003030743 Apr 2003 WO
2003065916 Aug 2003 WO
2003077769 Sep 2003 WO
2003090630 Nov 2003 WO
2004107989 Dec 2004 WO
2006042210 Apr 2006 WO
2007016290 Feb 2007 WO
2007026354 Mar 2007 WO
2007137304 Nov 2007 WO
2008131362 Oct 2008 WO
2008133956 Nov 2008 WO
2009039506 Mar 2009 WO
2007014355 Apr 2009 WO
2009132359 Oct 2009 WO
2009143092 Nov 2009 WO
2009149234 Dec 2009 WO
2011108840 Sep 2011 WO
2012040984 Apr 2012 WO
Non-Patent Literature Citations (28)
Entry
Extended European Search Report corresponding to International Application No. EP 15 15 1076.5 dated Apr. 22, 2015.
Japanese Office Action corresponding to International Application No. JP 2011-084092 dated Jan. 14, 2016.
Extended European Search Report corresponding to International Application No. EP 12 19 7970.2 dated Jan. 28, 2016.
Chinese Office Action corresponding to International Application No. CN 201210560638.1 dated Oct. 21, 2015.
European Office Action corresponding to International Application No. EP 14 15 9056.2 dated Oct. 26, 2015.
Australian Examination Report No. 1 corresponding to International Application No. AU 2015200153 dated Dec. 11, 2015.
Australian Examination Report No. 1 corresponding to International Application No. AU 2014204542 dated Jan. 7, 2016.
Chinese Office Action corresponding to International Application No. CN 201310125449.6 dated Feb. 3, 2016.
Extended European Search Report corresponding to International Application No. EP 15 19 0245.9 dated Jan. 28, 2016.
Extended European Search Report corresponding to International Application No. EP 15 16 7793.7 dated Apr. 5, 2016.
European Office Action corresponding to International Application No. EP 14 18 4882.0 dated Apr. 25, 2016.
Extended European Search Report corresponding to International Application No. EP 14 19 6704.2 dated Sep. 24, 2015.
International Search Report and Written Opinion corresponding to Int'l Appln. No. PCT/US2015/051837, dated Dec. 21, 2015.
Extended European Search Report corresponding to International Application No. EP 14 19 7563.1 dated Aug. 5, 2015.
Partial European Search Report corresponding to International Application No. EP 15 19 0643.5 dated Feb. 26, 2016.
Extended European Search Report corresponding to International Application No. EP 15 16 6899.3 dated Feb. 3, 2016.
Extended European Search Report corresponding to International Application No. EP 14 19 9783.3 dated Dec. 22, 2015.
Extended European Search Report corresponding to International Application No. EP 15 17 3807.7 dated Nov. 24, 2015.
Extended European Search Report corresponding to International Application No. EP 15 19 0760.7 dated Apr. 1, 2016.
Extended European Search Report corresponding to International Application No. EP 15 17 3803.6 dated Nov. 24, 2015.
Extended European Search Report corresponding to International Application No. EP 15 17 3804.4 dated Nov. 24, 2015.
Extended European Search Report corresponding to International Application No. EP 15 18 8539.9 dated Feb. 17, 2016.
Extended European Search Report corresponding to International Application No. EP 15 17 3910.9 dated Nov. 13, 2015.
European Office Action corresponding to International Application No. EP 14 15 2236.7 dated Aug. 11, 2015.
Extended European Search Report corresponding to International Application No. EP 15 18 4915.5 dated Jan. 5, 2016.
European Search Report No. 14185097.4 dated Jan. 27, 2015.
European Search Report No. 13189650.8 dated Sep. 10, 2014.
Chinese Office Action dated Oct. 24, 2017 in corresponding Chinese Patent Application No. 201410479971.9 together with English translation, 12 pages.
Related Publications (1)
Number Date Country
20150076206 A1 Mar 2015 US
Provisional Applications (1)
Number Date Country
61879445 Sep 2013 US