This invention relates to a tissue biopsy sampling device. More specifically, the invention relates to mechanical features of an automatic biopsy sampling device.
Often, it is either desirable or necessary to obtain specimens of tissue from humans and other animals, particularly in the diagnosis and treatment of patients with cancerous tumors, premalignant conditions, and other diseases or disorders. For example, when it is discovered that suspicious conditions exist, either by means of x-ray or ultrasound imaging in various tissues of the body, a physician typically performs a biopsy to determine if the cells at the suspected site are cancerous.
A biopsy can be done either by an open or percutaneous technique. Open biopsy is an invasive procedure using a scalpel, whereby either a portion (incisional biopsy) or the entire mass (excisional biopsy) is removed. Percutaneous biopsy is usually done with a needle-like instrument through a relatively small incision, and can be performed by fine needle aspiration (FNA) or through the taking of a core biopsy sample. In FNA biopsy, individual cells or clusters of cells are obtained for cytologic examination and can be prepared such as in a Papanicolaou smear. In a core biopsy, a core or fragment of the tissue is obtained for histologic examination.
Intact tissue from the organ, lesion, or tumor is preferred by medical personnel in order to arrive at a definitive diagnosis regarding the patient's condition. In most cases only part of the tissue in question needs to be sampled. The portions of tissue extracted must be indicative of the organ, lesion, or tumor as a whole. Often, multiple tissue samples from various locations of the mass being sampled may be taken.
The percutaneous biopsy procedure can be performed utilizing various techniques and devices. An example is a method and a device that employs a biopsy needle for cutting tissue sample as described in British Patent Publication No. GB 2018601A. In the described biopsy device, living tissue is sucked into a cutting region under vacuum. The vacuum is created in the needle by employing connecting lines to a vacuum generator situated outside of a hand piece that holds the cannula. The cutting of the sample is done using a cutting mechanism that moves axially over the cannula. After sampling, the needle is withdrawn from the host and the sample is flushed out from the tip of the needle. The vacuum established in the hollow needle is regulated externally from the hand-piece.
Another biopsy mechanism is described in European Patent Publication No. EP 0890 339 A1. A biopsy needle with a cutting mechanism is integrated into a hand piece. The needle is connected via connections lines to an external vacuum generator and controls. The cutting device is moveable axially in the hollow space of the biopsy needle. A rotary movement, combined with a manual lengthwise push causes the cutting device to sample the tissue from the host. The sample is transported in the hollow channel of the needle. A similar arrangement is also shown by U.S. Pat. No. 5,526,822. In these devices, the vacuum generation mechanisms and controls are costly and tend to be provided in permanent fixtures that are separate from the disposable components. A manual biopsy device is known from German Patent No. DE 40 41 614 C1. In this device, a partial vacuum source is provided by a piston and cylinder pump. A similar partial vacuum-assisted biopsy device can be found in International Publication No. WO 96/28097, which has a syringe plunger arrangement located inside a manual device to create partial vacuum.
A vacuum-assisted biopsy device is described in U.S. Patent Publication No. 2001/0011156 A1, provides for a compactly configured hand device, in whose housing all drive elements necessary for propelling the needle of the biopsy needle arrangement are provided. However, a partial vacuum source is provided separate from the hand device, which can be connected via an appropriate supply line to the needle arrangement inside the hand device at a suitable connection location.
U.S. Pat. No. 20050203439, hereby incorporated herein by reference in its entirety, describes a biopsy device for taking tissue samples, which includes a housing, a removable element and a control panel. The removable part has a vacuum pump in the form of a syringe which is driven by a first motor and a biopsy needle which is driven by a separate motor under the control of a controller built into a permanent hand set. The needle and syringe are provided as a sterile package unit.
There is a need for improvements in biopsy devices that provide for high performance with low manufacturing cost, simplicity, reliability, and ease of use. Current devices are complex, either requiring many parts such as motors and drive components or providing low performance such as weak low penetration force, small sample size, poor sample integrity, etc. There is a need for design features that permit a biopsy device to be fully automated, yet fully disposable as well as economical, susceptible to efficient manufacture, simple, and reliable.
The embodiments disclosed herein relate to self-contained hand-held biopsy needles with various features relating to automated sampling and recovery. Among the disclosed features are ones suited to fully-disposable single-use automatic biopsy devices, such as light weight, low cost, and simple design.
According to an embodiment, a biopsy device is provided which has a housing and a biopsy needle projecting from the housing. The biopsy needle has a first member that defines a sample chamber and a second member that defines a sample volume within the sample chamber. A pump generates a vacuum in the sample volume. A primary drive element has a first drive interval and a second drive interval. A first transmission is driven by the primary drive element during the first drive interval to operate the pump and a second transmission driven by the primary drive element during the second drive interval to position the first and second members of the biopsy needle to define the sample volume.
Preferably, a housing encloses the pump, the primary drive element, the first transmission, the second transmission, and a portion of the biopsy needle. The first and second drive intervals are sequential. The first drive interval overlaps the second drive interval. The second drive interval follows after the start of the first drive interval. The first and second drive intervals are physical displacement intervals. The first and second drive intervals have identical endpoints and the second drive interval begins after the beginning of the first drive interval. The device includes a motor with an output connected to the primary drive element and a controller selectively operates the motor in forward and reverse directions.
According to another embodiment a biopsy device is provided which has a biopsy needle with tissue-penetration and tissue-sampling configurations. A pump is connected to the biopsy needle to generate a vacuum in the biopsy needle. A first drive element is connected to operate the pump. A second drive element is provided to configure the biopsy needle. The first drive element has a first displacement interval and a second displacement interval such that during the first displacement interval, the first drive element operates the pump to generate a vacuum in the biopsy needle, and during the second displacement interval, the first drive element engages the second drive element to configure the biopsy needle into the tissue-sampling configuration.
Preferably, the second displacement interval follows the first displacement interval. Also, preferably, the first displacement interval overlaps the second displacement interval. Also, preferably, the second displacement interval follows after the start of the first displacement interval. The first and second displacement intervals can have the same endpoints and the second displacement interval preferably starts after the start of the first displacement interval. Preferably, a motor provides an output connected to the first drive element and a controller selectively operates the motor in forward and reverse directions. Also, preferably, a housing encloses the pump, the first and second drive elements, and a portion of the biopsy needle.
According to another embodiment a biopsy device is provided which has a biopsy needle selectively configurable into a sampling configuration for creating a tissue sample and an insertion/removal configuration for inserting or extracting the biopsy needle from living tissue. A pump connected to the biopsy needle generates a vacuum therein. A first drive element is provided which is connected to drive the pump. A second drive element is also connected to configure the biopsy needle. A primary drive member is displaced through a continuous range having a first interval and a second interval. During the first interval, a motive force is transmitted through the primary drive member to the first drive element to cause the pump to generate a vacuum and, during the second interval, a motive force is transmitted to the second drive element to configure the biopsy needle from the insertion/removal configuration to the sampling configuration. During the second interval, a motive force continues to be transmitted to the first drive element to cause the pump to continue generating a vacuum. Preferably, the continuous range has a third interval, following the second interval, during which the second drive element configures the biopsy needle from the sampling configuration to the insertion/withdrawal configuration. Also, preferably, the first drive element is spaced apart from the second drive element such that the primary drive member engages the first drive element during the first interval and, as it moves toward the second drive element, engages the second drive element during the second interval.
According to another embodiment a biopsy device is provided which has a biopsy needle selectively configurable into a cutting configuration, for cutting a tissue sample, and an insertion configuration, for insertion into a host. A pump is connected to the biopsy needle to generate a vacuum therein. A prime mover is provided with a primary output element, which can be displaced through first and second intervals. A transmission mechanism is connected to the primary output element. The transmission mechanism has at least a first transmission output to configure the biopsy needle and at least a second transmission output to operate the pump. The transmission mechanism is configured to cause the pump to generate a vacuum during a first displacement of the primary output element and to configure the biopsy needle from the insertion configuration to the cutting configuration during a second displacement of the primary output element. Preferably, the transmission mechanism includes a first drive element and a second drive element spaced apart therefrom. Also, preferably, the first and second drive elements drive the first and second transmission outputs, respectively. In this case, the primary output element is arranged to drive the first drive element during the first displacement and to move at least one of the first drive element and the primary drive element toward the second drive element until it engages and drives the second drive element and thereafter drive the second drive element during the second displacement.
According to another embodiment a biopsy device is provided which has a biopsy needle that is selectively configurable into a sampling configuration and an insertion configuration. The device has a pump connected to the biopsy needle to generate a vacuum therein. A motor and a transmission mechanism is provided where the transmission mechanism is configured to transmit motive force from the motor to the pump during a first interval upon activation of the motor, and, during a second interval, following the first interval, to transmit motive force from the motor to the biopsy needle to change its configuration from the insertion configuration to the sampling configuration such that a substantial vacuum is generated by the pump before the biopsy needle is configured into the sampling configuration. Preferably, the motor operates continuously during the first and second intervals. More preferably, both the pump and the motor operate continuously during the first and second intervals. In an embodiment, the pump is operates continuously during the first and second intervals.
The sampling configuration can include a continuous cycle that includes receiving a tissue sample within the biopsy needle and cutting the tissue sample from a host. The biopsy needle has fixed shaft, a longitudinal axis, and a rotating shaft movably connected to the fixed shaft to rotate around the longitudinal axis. The rotating shaft can include a cutting blade to cut tissue samples. The sampling configuration can also include a continuous sampling cycle, during the second interval, in which a tissue sample is cut and received within the biopsy needle, the transmission mechanism being configured to urge the rotating shaft progressively during the second interval to cut a tissue sample and cause it to be received in the biopsy needle.
According to another embodiment a biopsy device is provided which has a biopsy needle, selectively configurable into a sample access configuration and an insertion configuration. The biopsy needle has a sample chamber. The device also has a pump connected to the sample chamber to generate a vacuum therein and a motor with a transmission mechanism. The transmission mechanism is connected to configure the biopsy needle and drive the pump, upon activation of the motor in a first direction. The transmission mechanism transmits motive force from the motor to the pump during a first interval and, as the motor continues during a second interval that follows the first interval, the transmission mechanism transmits motive force to the biopsy needle to change its configuration from the insertion configuration to the sample access configuration such that a substantial vacuum is generated in the sample chamber before the biopsy needle is configured into the sample access configuration.
Preferably, upon activation of the motor in a second direction, the transmission mechanism transmits a motive force from the motor to the pump during a third interval following the second interval and simultaneously change the biopsy needle configuration from the insertion configuration to the sample access configuration to generate pressure in the sample chamber to eject a sample therefrom. The pump is preferably operated during at least part of the second interval. Preferably, the pump is operated throughout the second interval. Also, preferably, a housing encloses the pump, the transmission mechanism, and a portion of the biopsy needle.
According to another embodiment a biopsy device is provided which has a biopsy needle with an elongate inner cylindrical member and an elongate outer cylindrical member, the outer cylindrical member being coaxially aligned with the inner cylindrical member and rotatable with respect to it. The inner cylindrical member has a port and the outer cylindrical member has a cover portion capable of being aligned with the port to cover it for insertion of the biopsy needle. The outer cylindrical member has a cutting edge adjacent to the cover portion such that, as the outer cylindrical member is rotated progressively about the inner cylindrical member through a specified interval, the cutting edge passes over the port and covers the port. The cutting edge and port is shaped such may as the outer cylindrical member rotates, a progressively greater fraction of the cutting edge passes over the port.
Preferably, the inner cylindrical member has a trocar affixed to a distal tip thereof. Preferably, also, the cutting edge has at least a portion that is angled relative to the perpendicular to the direction of advance of the cutting edge. The inner cylindrical member has a surface with at least one barb aligned with a port edge of the port opposite the cutting edge as the cutting edge advances toward the port edge prior to covering the port. The inner cylindrical member can have a sharp edge partly defining the port, the sharp edge having a portion extending toward the axis of the inner cylindrical member and opposite the cutting edge as the cutting edge advances toward the port edge prior to covering the port.
According to another embodiment a biopsy device is provided which has a housing that defines a chamber with a biopsy needle partially disposed in the chamber. The biopsy needle has a first member that defines a sample chamber and a second member may define a sample volume with the sample chamber. The device has a pump that generates a vacuum at the sample chamber and a primary drive element positioned with the housing. The primary drive element has a first drive interval and a sequential second drive interval. A first transmission driven by the primary drive element during the first drive interval operates the pump. A second transmission driven by the primary drive element during the second drive interval positions the first and second members of the biopsy needle to define the sample volume.
According to another embodiment a biopsy device is provided which has a biopsy needle with a sample chamber that has an access opening. The biopsy needle has a cover member movable relative to the access opening to cover the access opening. A pump is connected to the biopsy needle to generate a vacuum in the sample chamber. A drive element is provided that simultaneously drives the pump and moves the cover member relative to the access opening through a sampling cycle over which the pump generates a vacuum in the sample chamber and the cover member moves relative to the sample chamber through a delay interval in which the access opening remains covered by the cover member and through a sampling interval, following the delay interval, in which the access opening is uncovered. The cover member has a cutting edge which cuts a sample free of a host after the access opening is uncovered.
According to another embodiment, a biopsy device includes an elongate inner cylindrical member and an elongate outer cylindrical member. The outer cylindrical member is coaxially aligned with the inner cylindrical member and movable with respect to it along a common axis of the inner and outer cylindrical members. The inner cylindrical member has a port and the outer cylindrical member has a cover portion capable of being aligned with the port to cover it for insertion of the biopsy needle. A drive mechanism drives a first transmission member connected to a vacuum pump. The first transmission member drives a second transmission member connected to the outer cylindrical member to displace it without rotating it. The outer cylindrical member has a cutting edge adjacent to the cover portion such that, as the outer cylindrical member is displaced along the inner cylindrical member by the drive mechanism, the cutting edge passes over the port and covers the port. Preferably, the vacuum pump is connected to the inner cylindrical member to create a vacuum in communication with the port. The inner cylindrical member would ordinarily have a cutting tip, such as a trocar affixed to a distal tip thereof.
The accompanying drawings, which are incorporated herein and constitute part of this specification, illustrate presently preferred exemplary embodiments of the invention, and, together with the general description given above and the detailed description given below, serve to explain features of the invention.
While the biopsy needle is in the insertion position shown in
As the outer sheath 105 rotates toward the position shown in
To remove the tissue sample, the operation depicted in
Note that the outer sheath 105 could rotate in either direction, or both directions, in alternative embodiments. For example, the port 130 could be uncovered by rotating in one direction and the cutting operation and covering could occur after reversing the direction of rotation immediately after uncovering the port 130. This alternative may be provided for all of the embodiments described herein. In addition, the blade 120 may be on either or both sides of the opening 150.
The speed of rotation of the outer sheath 105 may be constant or variable. For example, to reduce or amplify torque from the drive mechanism, a reduced force/torque transmission ratio of the drive may be provided to level the prime mover load through the cutting phase.
Referring again to
The embodiment of
As mentioned, the embodiment of
While the biopsy needle is in the insertion position shown in
As the outer sheath 106 rotates toward the position shown in
To remove the tissue sample, the operation depicted in
Note that the outer sheath 106 could rotate in either direction with an appropriate repositioning of the blade 121. In addition, the blade 121 may be on both sides of the opening 151. As in the prior embodiment, the speed of rotation of the outer sheath 106 may be constant or variable to amplify torque from the drive mechanism. Referring again to
The movement of the outer sheath 105 or 106 of the foregoing embodiments may be permitted by providing that the inner sheath 135 or 136 be journaled within the outer sheath 105 or 106. A lubricant may or may not be provided.
Referring back to
While the biopsy needle is in the insertion position shown in
As the outer sheath 205 rotates toward the position shown in
To remove the tissue sample, the operation depicted in
As in the previous embodiments, the outer sheath 205 could rotate in either direction, or both directions, in alternative embodiments. For example, the port 130 could be uncovered by rotating in one direction and the cutting operation and covering could occur after reversing the direction of rotation immediately after uncovering the port 130. This alternative may be provided for all of the embodiments described herein. In addition, the blade 220 may be on either or both sides of the opening 250. As in the previous embodiments, the speed of rotation of the outer sheath 205 may be constant or variable. For example, to reduce amplify torque from the drive mechanism, a reduced force/torque transmission ratio of the drive may be provided to level the prime mover load through the cutting phase. As in the prior embodiments, the port 130 may have angled edges (as has port 104 in the embodiment of
The embodiment of
While the biopsy needle is in the insertion position shown in
As the outer sheath 206 rotates toward the position shown in
To remove the tissue sample, the operation depicted in
As in the previous embodiments, the outer sheath 206 could rotate in either direction, or both directions, in alternative embodiments. For example, the port 231 could be uncovered by rotating in one direction and the cutting operation and covering could occur after reversing the direction of rotation immediately after uncovering the port 231. This alternative may be provided for all of the embodiments described herein. In addition, the blade 221 may be on either or both sides of the opening 251. As in the previous embodiments, the speed of rotation of the outer sheath 206 may be constant or variable. For example, to reduce amplify torque from the drive mechanism, a reduced force/torque transmission ratio of the drive may be provided to level the prime mover load through the cutting phase. As in the prior embodiments, the port 231 may be angled (as is 104 relative to 130 in
The embodiment of
In the foregoing embodiments, it is preferable for a substantial vacuum to be generated before the biopsy needle is actuated for cutting. This is so that a poor sample specimen does not result due to the cutting operation getting underway before the tissue sample is drawn well into the sample chamber. This can be ensured in a variety of ways, for example by providing a drive system with independently controlled vacuum source and biopsy needle that are sequenced to generate the vacuum before the biopsy needle is placed into a configuration for sampling.
Referring now to
The vacuum is preferably established when the sample chamber is uncovered. This may ensure that the severing operation can be completed and the sample secured without the sample chamber being open for a long interval. In principle this is not essential, but in practice it may be desirable for various reasons: (1) an imperfect fluid seal may exist so that a progressive vacuum may not reach a desired peak level; (2) excess fluid may be drawn from the host, thereby compromising the vacuum and producing an undesirable result when a solid specimen is required; and (3) excessive fluid may be accumulated in the tissue sample due to an extended exposure to the vacuum, while attached to the host. Other effects such as compliance in the biopsy device's fluid circuit and other factors may also favor an operating sequence in which the host is exposed to the vacuum as briefly as possible. In all of the disclosed embodiments, means of anchoring tissue samples other than vacuum may be employed. For example, external pressure on the host tissue from outside the patient body (e.g. by means of a tissue compression device or manual pressure by the practitioner) may be employed alone, or in addition to vacuum, for forcing samples into the sample chamber.
The time during which a vacuum pump is operated to create the pressure curve, shown at 408, is indicated by the bar 402. For the entire period t0 to t5, a vacuum pump may be operated. At a point after a substantial vacuum is generated, for example t2, the sample opening (e.g., as port 130 in
The above sequencing may be achieved by employing independent drive mechanisms for the vacuum and biopsy needle. In a design suitable for a disposable biopsy needle it may be preferred to have a single drive system that can achieve the same operation sequence as just described in a manner that is reliable, with a simple a structure and low cost, by employing a single mechanical drive, as discussed below.
An embodiment of a biopsy needle 448, similar to the embodiment of
In the series of figures,
It will be observed that the above operation of the needle 448 and pump 480 is effective to provide the sequencing of the vacuum creation and sampling cycle described above with reference to
Referring again to
The mechanism of
Depending on the desired timing, both the pump 480 and the outer sheath may be moved in a reverse direction during the sample-ejection cycle, which may allow a simpler driving system. For example, if the initial and final positions of the outer sheath 450 are as shown in
Referring now to
In the foregoing mechanism, it is possible to allow the pump 712 to disengage from the prime mover output 702 at a desired point in the cycle. This may be desirable to level the load on the prime mover 700 so that it does not require the capacity to operate the pump 712 and the sampling device 714, simultaneously.
Referring now to
Referring now to
The rack 510 engages a pinion 514 which has a driving bevel gear 516 that engages a driven bevel gear 518. The driven bevel gear 518 is affixed to a sheath driving gear 520 which engages a sheath driven gear affixed concentrically to the outer sheath 526. The sample chamber is exposed, and a sample is cut, when an opening 528 in the outer sheath 526 is rotated by the sheath driven gear 522 at a point in time when the rack 510 engages the pinion 514.
During a sampling procedure, the motor is run continuously in a single direction causing the rack 510 to advance to the right, driven by the screw gear 507. As the rack 510 moves to the right as illustrated in
The mechanism used to displace the rack 510 can be any suitable mechanism. For example a pinion gear 574 may be used with a drive motor 572 which may itself include a gear train, such as a planetary gear, to amplify torque. Another example is a worm gear 576 as illustrated driven by a suitably arranged motor 570.
Referring now to
The biopsy needle 618 has an outer sheath 623 and an inner sheath 637. The outer sheath 623 rotates around the inner sheath 637 to bring an opening 620 in the outer sheath 623 into coincidence with an opening 621 in the inner sheath 637 and perform a cutting operation as the outer sheath. A pin 624 is affixed to the outer sheath 623 which can rotate around the inner sheath 637.
A pushrod 602 is connected to the threaded rod 608 and is open at the bottom to define a channel 604 so that the pushrod 602 can move without interfering with the tube 606. The pushrod displaces a cam drive 630 with a slot 631. The slot 631 has a helical portion 626 and a straight portion 638. A pin 624 is affixed to the outer sheath 623 and engaged in the slot 631. The cam drive 630 moves to the right as the piston 607 is displaced, the cam drive 630 being moved by the piston 607, threaded rod 608, pushrod 602, all of which move together. During an initial displacement of the piston 607, in which a vacuum is generated, the straight portion 638 of the slot 631 allows the cam drive 630 to move without affecting the position of the pin 624. When the helical portion 626 of the slot 631 reaches the pin 624, however, the outer sheath 623 is rotated as the piston 607 continues to be displaced. In this way, the cam drive 630 provides for an operation that is similar to that of
A pivot arm 933 is pivotally connected to the carriage 907 about a first end 939 thereof. A spring 943 generates a torque between a pivot arm 933 and a boss 905 on the carriage 907 to keep the free end 935 in engagement with a shelf 937. As the carriage 907 moves, rides along the shelf 937, from the position shown in
The cutting sheath 921 is further retracted as the carriage 907 moves further while the free end 935 slides up a ramp portion 927 of the shelf 937 as shown in
In any of the foregoing embodiments, the motors or prime movers disclosed in each embodiment may be replaced by rotary or linear motors which may be driven by electromotive force, by spring motors, hydraulic of pneumatic motors, thermal motors, or by any means of generating a motive force. Different types of displacement (e.g., rotary or linear) can be mapped to the required forms by means of suitable transmissions according to well-known techniques of kinematic design. For example, although the embodiment of
The above-disclosed embodiments may provide at least one of a variety of advantages including:
While the present invention has been disclosed with reference to certain preferred exemplary embodiments, numerous modifications, alterations, and changes to the described exemplary embodiments are possible without departing from the sphere and scope of the present invention. Accordingly, it is intended that the present invention not be limited to the described exemplary embodiments, but that it have the full scope.
This application is a U.S. nation phase of International Application No. PCT/US2007/076214, filed Aug. 17, 2007 which claims priority to U.S. Provisional Application Ser. No. 60/823,038, filed Aug. 21, 2006, hereby incorporated by reference in its entirety.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US2007/076214 | 8/17/2007 | WO | 00 | 2/19/2009 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2008/024684 | 2/28/2008 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 737293 | Summerteldt | Aug 1903 | A |
| 1585934 | Muir | Dec 1923 | A |
| 1663761 | Johnson | Feb 1927 | A |
| 2953934 | Sundt | Sep 1960 | A |
| 3019733 | Braid | Feb 1962 | A |
| 3224434 | Molomut et al. | Dec 1965 | A |
| 3477423 | Griffith | Jan 1967 | A |
| 3512519 | Hall | Oct 1967 | A |
| 3561429 | Jewett et al. | Feb 1971 | A |
| 3565074 | Foti | Feb 1971 | A |
| 3606878 | Kellogg | Sep 1971 | A |
| 3727602 | Hyden et al. | Apr 1973 | A |
| 3732858 | Banko | May 1973 | A |
| 3800783 | Jamshidi | Apr 1974 | A |
| 3844272 | Banko | Oct 1974 | A |
| 3882849 | Jamshidi | May 1975 | A |
| 4275730 | Hussein | Jun 1981 | A |
| 4282884 | Boebel | Aug 1981 | A |
| 4306570 | Matthews | Dec 1981 | A |
| 4354092 | Manabe et al. | Oct 1982 | A |
| 4445509 | Auth | May 1984 | A |
| 4490137 | Moukheibir | Dec 1984 | A |
| 4549554 | Markham | Oct 1985 | A |
| 4577629 | Martinez | Mar 1986 | A |
| 4589414 | Yoshida et al. | May 1986 | A |
| 4603694 | Wheeler | Aug 1986 | A |
| 4605011 | Naslund | Aug 1986 | A |
| 4617430 | Bryant | Oct 1986 | A |
| 4620539 | Andrews et al. | Nov 1986 | A |
| 4643197 | Greene et al. | Feb 1987 | A |
| 4645153 | Granzow et al. | Feb 1987 | A |
| 4678459 | Onik et al. | Jul 1987 | A |
| 4696298 | Higgins et al. | Sep 1987 | A |
| 4702260 | Wang | Oct 1987 | A |
| 4776346 | Beraha et al. | Oct 1988 | A |
| 4844087 | Garg | Jul 1989 | A |
| 4850354 | McGurk-Burleson et al. | Jul 1989 | A |
| 4893635 | de Groot et al. | Jan 1990 | A |
| 4907598 | Bauer | Mar 1990 | A |
| 33258 | Onik et al. | Jul 1990 | A |
| RE33258 | Onik et al. | Jul 1990 | E |
| 4940061 | Terwilliger et al. | Jul 1990 | A |
| 4952817 | Bolan et al. | Aug 1990 | A |
| 4958625 | Bates et al. | Sep 1990 | A |
| 4967762 | DeVries | Nov 1990 | A |
| 4986278 | Ravid et al. | Jan 1991 | A |
| 4986279 | O'Neill | Jan 1991 | A |
| 4986807 | Farr | Jan 1991 | A |
| 4989614 | Dejter, Jr. et al. | Feb 1991 | A |
| 5025797 | Baran | Jun 1991 | A |
| 5125413 | Baran | Jun 1992 | A |
| 5138245 | Mattinger et al. | Aug 1992 | A |
| 5146921 | Terwilliger et al. | Sep 1992 | A |
| 5158528 | Walker et al. | Oct 1992 | A |
| 5176628 | Charles et al. | Jan 1993 | A |
| 5225763 | Krohn et al. | Jul 1993 | A |
| 5234000 | Hakky et al. | Aug 1993 | A |
| 5236334 | Bennett | Aug 1993 | A |
| 5249583 | Mallaby | Oct 1993 | A |
| 5282476 | Terwilliger | Feb 1994 | A |
| 5282477 | Bauer | Feb 1994 | A |
| 5324306 | Makower et al. | Jun 1994 | A |
| 5334183 | Wuchinich | Aug 1994 | A |
| 5368029 | Holcombe et al. | Nov 1994 | A |
| 5368045 | Clement et al. | Nov 1994 | A |
| 5400798 | Baran | Mar 1995 | A |
| 5439474 | Li | Aug 1995 | A |
| 5458112 | Weaver | Oct 1995 | A |
| 5469860 | De Santis | Nov 1995 | A |
| 5479486 | Saji | Dec 1995 | A |
| 5485917 | Early | Jan 1996 | A |
| 5492130 | Chiou | Feb 1996 | A |
| 5511556 | DeSantis | Apr 1996 | A |
| 5526822 | Burbank et al. | Jun 1996 | A |
| 5535755 | Heske | Jul 1996 | A |
| 5546957 | Heske | Aug 1996 | A |
| 5554151 | Hinchliffe | Sep 1996 | A |
| 5560373 | De Santis | Oct 1996 | A |
| 5564436 | Hakky et al. | Oct 1996 | A |
| 5569284 | Young et al. | Oct 1996 | A |
| 5575293 | Miller et al. | Nov 1996 | A |
| 5591170 | Spievack et al. | Jan 1997 | A |
| 5601585 | Banik et al. | Feb 1997 | A |
| 5602449 | Krause et al. | Feb 1997 | A |
| 5617874 | Baran | Apr 1997 | A |
| 5649547 | Ritchart et al. | Jul 1997 | A |
| 5655542 | Weilandt | Aug 1997 | A |
| 5655657 | Roshdy | Aug 1997 | A |
| 5665101 | Becker et al. | Sep 1997 | A |
| 5669394 | Bergey et al. | Sep 1997 | A |
| 5699909 | Foster | Dec 1997 | A |
| 5700265 | Romano | Dec 1997 | A |
| 5709697 | Ratcliff et al. | Jan 1998 | A |
| 5720760 | Becker et al. | Feb 1998 | A |
| 5735264 | Siczek et al. | Apr 1998 | A |
| 5752923 | Terwilliger | May 1998 | A |
| 5755714 | Murphy-Chutorian | May 1998 | A |
| 5766135 | Terwilliger | Jun 1998 | A |
| 5769086 | Ritchart et al. | Jun 1998 | A |
| 5769795 | Terwilliger | Jun 1998 | A |
| 5775333 | Burbank et al. | Jul 1998 | A |
| 5788651 | Weilandt | Aug 1998 | A |
| 5792167 | Kablik et al. | Aug 1998 | A |
| 5807282 | Fowler | Sep 1998 | A |
| 5817033 | DeSantis et al. | Oct 1998 | A |
| 5817034 | Milliman et al. | Oct 1998 | A |
| 5823970 | Terwilliger | Oct 1998 | A |
| 5827305 | Gordon | Oct 1998 | A |
| 5830219 | Bird et al. | Nov 1998 | A |
| D403405 | Terwilliger | Dec 1998 | S |
| 5857982 | Milliman et al. | Jan 1999 | A |
| 5879365 | Whitfield et al. | Mar 1999 | A |
| 5908233 | Heskett et al. | Jun 1999 | A |
| 5913857 | Ritchart et al. | Jun 1999 | A |
| 5916198 | Dillow | Jun 1999 | A |
| 5916229 | Evans | Jun 1999 | A |
| 5928164 | Burbank et al. | Jul 1999 | A |
| 5944673 | Gregoire et al. | Aug 1999 | A |
| 5951490 | Fowler | Sep 1999 | A |
| 5951575 | Bolduc et al. | Sep 1999 | A |
| 5964716 | Gregoire et al. | Oct 1999 | A |
| 5971939 | DeSantis et al. | Oct 1999 | A |
| 5976164 | Bencini et al. | Nov 1999 | A |
| 5980469 | Burbank et al. | Nov 1999 | A |
| 5980545 | Pacala et al. | Nov 1999 | A |
| 6007495 | Matula | Dec 1999 | A |
| 6007497 | Huitema | Dec 1999 | A |
| 6007556 | Kablik et al. | Dec 1999 | A |
| 6017316 | Ritchart et al. | Jan 2000 | A |
| 6018227 | Kumar et al. | Jan 2000 | A |
| 6019733 | Farascioni | Feb 2000 | A |
| 6022324 | Skinner | Feb 2000 | A |
| 6022325 | Siczek et al. | Feb 2000 | A |
| 6027458 | Janssens | Feb 2000 | A |
| 6036657 | Milliman et al. | Mar 2000 | A |
| 6050955 | Bryan et al. | Apr 2000 | A |
| 6077230 | Gregoire et al. | Jun 2000 | A |
| 6083176 | Terwilliger | Jul 2000 | A |
| 6083237 | Huitema et al. | Jul 2000 | A |
| 6086544 | Hibner et al. | Jul 2000 | A |
| 6106484 | Terwilliger | Aug 2000 | A |
| 6110129 | Terwilliger | Aug 2000 | A |
| 6120462 | Hibner et al. | Sep 2000 | A |
| 6123957 | Jernberg | Sep 2000 | A |
| 6126617 | Weilandt et al. | Oct 2000 | A |
| 6142955 | Farascioni et al. | Nov 2000 | A |
| 6162187 | Buzzard et al. | Dec 2000 | A |
| 6165136 | Nishtala | Dec 2000 | A |
| 6193673 | Viola et al. | Feb 2001 | B1 |
| 6196978 | Weilandt et al. | Mar 2001 | B1 |
| 6213957 | Milliman et al. | Apr 2001 | B1 |
| 6220248 | Voegele et al. | Apr 2001 | B1 |
| 6231522 | Voegele et al. | May 2001 | B1 |
| 6241687 | Voegele et al. | Jun 2001 | B1 |
| 6267759 | Quick | Jul 2001 | B1 |
| 6273861 | Bates et al. | Aug 2001 | B1 |
| 6273862 | Privitera et al. | Aug 2001 | B1 |
| 6280398 | Ritchart et al. | Aug 2001 | B1 |
| 6283925 | Terwilliger | Sep 2001 | B1 |
| 6322523 | Weilandt et al. | Nov 2001 | B2 |
| 6328701 | Terwilliger | Dec 2001 | B1 |
| 6331166 | Burbank et al. | Dec 2001 | B1 |
| 6358217 | Bourassa | Mar 2002 | B1 |
| 6402701 | Kaplan et al. | Jun 2002 | B1 |
| 6419641 | Mark et al. | Jul 2002 | B1 |
| 6428486 | Ritchart et al. | Aug 2002 | B2 |
| 6428487 | Burdorff et al. | Aug 2002 | B1 |
| 6432064 | Hibner et al. | Aug 2002 | B1 |
| 6432065 | Burdorff et al. | Aug 2002 | B1 |
| 6436054 | Viola et al. | Aug 2002 | B1 |
| 6482158 | Mault | Nov 2002 | B2 |
| 6485436 | Truckai et al. | Nov 2002 | B1 |
| 6488636 | Bryan et al. | Dec 2002 | B2 |
| 6527736 | Attinger et al. | Mar 2003 | B1 |
| 6540694 | Van Bladel et al. | Apr 2003 | B1 |
| 6540761 | Houser | Apr 2003 | B2 |
| 6551255 | Van Bladel et al. | Apr 2003 | B2 |
| 6554779 | Viola et al. | Apr 2003 | B2 |
| 6585664 | Burdorff et al. | Jul 2003 | B2 |
| 6585694 | Smith et al. | Jul 2003 | B1 |
| 6638235 | Miller et al. | Oct 2003 | B2 |
| 6656133 | Voegele et al. | Dec 2003 | B2 |
| 6659105 | Burbank et al. | Dec 2003 | B2 |
| 6659338 | Dittmann et al. | Dec 2003 | B1 |
| 6683439 | Takano et al. | Jan 2004 | B2 |
| 6689072 | Kaplan et al. | Feb 2004 | B2 |
| 6695786 | Wang et al. | Feb 2004 | B2 |
| 6712773 | Viola | Mar 2004 | B1 |
| 6712774 | Voegele et al. | Mar 2004 | B2 |
| 6752768 | Burdorff et al. | Jun 2004 | B2 |
| 6753671 | Harvey | Jun 2004 | B1 |
| 6758824 | Miller et al. | Jul 2004 | B1 |
| 6764495 | Lee et al. | Jul 2004 | B2 |
| 6832990 | Kortenbach et al. | Dec 2004 | B2 |
| 6849080 | Lee et al. | Feb 2005 | B2 |
| 6908440 | Fisher | Jun 2005 | B2 |
| D508458 | Solland et al. | Aug 2005 | S |
| 6926676 | Turturro et al. | Aug 2005 | B2 |
| 6984213 | Horner et al. | Jan 2006 | B2 |
| 7025732 | Thompson et al. | Apr 2006 | B2 |
| D525583 | Vu | Jul 2006 | S |
| 7153274 | Stephens et al. | Dec 2006 | B2 |
| 7189206 | Quick et al. | Mar 2007 | B2 |
| 7189207 | Viola | Mar 2007 | B2 |
| 7219867 | Kalis et al. | May 2007 | B2 |
| 7226424 | Ritchart et al. | Jun 2007 | B2 |
| 7276032 | Hibner | Oct 2007 | B2 |
| 7328794 | Lubs et al. | Feb 2008 | B2 |
| 7347829 | Mark et al. | Mar 2008 | B2 |
| 7374544 | Freeman et al. | May 2008 | B2 |
| 7397654 | Mori | Jul 2008 | B2 |
| 7402140 | Spero et al. | Jul 2008 | B2 |
| 7405536 | Watts | Jul 2008 | B2 |
| 7407054 | Seiler et al. | Aug 2008 | B2 |
| 7432813 | Postma | Oct 2008 | B2 |
| 7452367 | Rassman et al. | Nov 2008 | B2 |
| 7464040 | Joao | Dec 2008 | B2 |
| 7473232 | Teague | Jan 2009 | B2 |
| 7481775 | Weikel, Jr. et al. | Jan 2009 | B2 |
| 7490048 | Joao | Feb 2009 | B2 |
| 7513877 | Viola | Apr 2009 | B2 |
| 7517321 | McCullough et al. | Apr 2009 | B2 |
| 7517322 | Weikel, Jr. et al. | Apr 2009 | B2 |
| 7648466 | Stephens et al. | Jan 2010 | B2 |
| 7670299 | Beckman et al. | Mar 2010 | B2 |
| 7717861 | Weikel et al. | May 2010 | B2 |
| 7727164 | Cicenas et al. | Jun 2010 | B2 |
| 7740594 | Hibner | Jun 2010 | B2 |
| 7740596 | Hibner | Jun 2010 | B2 |
| 7740597 | Cicenas et al. | Jun 2010 | B2 |
| 7762961 | Heske et al. | Jul 2010 | B2 |
| 7828746 | Teague | Nov 2010 | B2 |
| 7854706 | Hibnner | Dec 2010 | B2 |
| 7883476 | Miller et al. | Feb 2011 | B2 |
| 20010007925 | Ritchart et al. | Jul 2001 | A1 |
| 20010011156 | Viola et al. | Aug 2001 | A1 |
| 20010012919 | Terwilliger | Aug 2001 | A1 |
| 20010014779 | Burbank et al. | Aug 2001 | A1 |
| 20010034530 | Malackowski et al. | Oct 2001 | A1 |
| 20010044595 | Reydel et al. | Nov 2001 | A1 |
| 20010047183 | Privitera et al. | Nov 2001 | A1 |
| 20020045840 | Voegele et al. | Apr 2002 | A1 |
| 20020065474 | Viola | May 2002 | A1 |
| 20020067151 | Tanishita | Jun 2002 | A1 |
| 20020068878 | Jasonni et al. | Jun 2002 | A1 |
| 20020082518 | Weiss et al. | Jun 2002 | A1 |
| 20020107043 | Adamson et al. | Aug 2002 | A1 |
| 20020120212 | Ritchart et al. | Aug 2002 | A1 |
| 20020151822 | Burdorff et al. | Oct 2002 | A1 |
| 20020156395 | Stephens et al. | Oct 2002 | A1 |
| 20030130593 | Gonzalez | Jul 2003 | A1 |
| 20030130677 | Whitman et al. | Jul 2003 | A1 |
| 20030163142 | Paltieli et al. | Aug 2003 | A1 |
| 20030229293 | Hibner et al. | Dec 2003 | A1 |
| 20030233101 | Lubock et al. | Dec 2003 | A1 |
| 20040015079 | Berger et al. | Jan 2004 | A1 |
| 20040019297 | Angel | Jan 2004 | A1 |
| 20040030367 | Yamaki et al. | Feb 2004 | A1 |
| 20040049128 | Miller et al. | Mar 2004 | A1 |
| 20040054299 | Burdorff et al. | Mar 2004 | A1 |
| 20040092992 | Adams et al. | May 2004 | A1 |
| 20040186393 | Leigh et al. | Sep 2004 | A1 |
| 20040215103 | Mueller, Jr. et al. | Oct 2004 | A1 |
| 20040220495 | Cahir et al. | Nov 2004 | A1 |
| 20040249278 | Krause | Dec 2004 | A1 |
| 20040267157 | Miller et al. | Dec 2004 | A1 |
| 20050004492 | Burbank et al. | Jan 2005 | A1 |
| 20050004559 | Quick et al. | Jan 2005 | A1 |
| 20050010131 | Burbank et al. | Jan 2005 | A1 |
| 20050020909 | Moctezuma de la Barrera et al. | Jan 2005 | A1 |
| 20050027210 | Miller | Feb 2005 | A1 |
| 20050049489 | Foerster et al. | Mar 2005 | A1 |
| 20050049521 | Miller et al. | Mar 2005 | A1 |
| 20050080355 | Mark | Apr 2005 | A1 |
| 20050085838 | Thompson et al. | Apr 2005 | A1 |
| 20050101879 | Shidham et al. | May 2005 | A1 |
| 20050113715 | Scwindt et al. | May 2005 | A1 |
| 20050113716 | Mueller, Jr. et al. | May 2005 | A1 |
| 20050124914 | Dicarlo et al. | Jun 2005 | A1 |
| 20050124915 | Eggers et al. | Jun 2005 | A1 |
| 20050165328 | Heske et al. | Jul 2005 | A1 |
| 20050177117 | Crocker et al. | Aug 2005 | A1 |
| 20050193451 | Quistgaard et al. | Sep 2005 | A1 |
| 20050203439 | Heske et al. | Sep 2005 | A1 |
| 20050209530 | Pflueger | Sep 2005 | A1 |
| 20050275378 | Canino et al. | Dec 2005 | A1 |
| 20050277829 | Tsonton et al. | Dec 2005 | A1 |
| 20050277871 | Selis | Dec 2005 | A1 |
| 20060030784 | Miller et al. | Feb 2006 | A1 |
| 20060074344 | Hibner | Apr 2006 | A1 |
| 20060074345 | Hibner | Apr 2006 | A1 |
| 20060113958 | Lobert et al. | Jun 2006 | A1 |
| 20060116603 | Shibazaki et al. | Jun 2006 | A1 |
| 20060129063 | Thompson et al. | Jun 2006 | A1 |
| 20060173377 | McCullough et al. | Aug 2006 | A1 |
| 20060178666 | Cosman et al. | Aug 2006 | A1 |
| 20060184063 | Miller | Aug 2006 | A1 |
| 20060241515 | Jones et al. | Oct 2006 | A1 |
| 20060258956 | Haberstich et al. | Nov 2006 | A1 |
| 20070016101 | Feldman et al. | Jan 2007 | A1 |
| 20070027407 | Miller | Feb 2007 | A1 |
| 20070032741 | Hibner et al. | Feb 2007 | A1 |
| 20070073326 | Miller et al. | Mar 2007 | A1 |
| 20070090788 | Hansford et al. | Apr 2007 | A1 |
| 20070106176 | Mark et al. | May 2007 | A1 |
| 20070118049 | Viola | May 2007 | A1 |
| 20070149894 | Heske et al. | Jun 2007 | A1 |
| 20070161925 | Quick et al. | Jul 2007 | A1 |
| 20070167782 | Callahan et al. | Jul 2007 | A1 |
| 20070179401 | Hibner | Aug 2007 | A1 |
| 20070213590 | Squicciarini | Sep 2007 | A1 |
| 20070213630 | Beckman et al. | Sep 2007 | A1 |
| 20070213632 | Okazaki et al. | Sep 2007 | A1 |
| 20070219572 | Deck et al. | Sep 2007 | A1 |
| 20070236180 | Rodgers | Oct 2007 | A1 |
| 20070239067 | Hibner et al. | Oct 2007 | A1 |
| 20070255173 | Hibner | Nov 2007 | A1 |
| 20070270710 | Frass et al. | Nov 2007 | A1 |
| 20070276288 | Khaw | Nov 2007 | A1 |
| 20070287933 | Phan et al. | Dec 2007 | A1 |
| 20070293788 | Entrekin et al. | Dec 2007 | A1 |
| 20080004545 | Garrison | Jan 2008 | A1 |
| 20080007217 | Riley | Jan 2008 | A1 |
| 20080015429 | Tsonton et al. | Jan 2008 | A1 |
| 20080021487 | Heisler | Jan 2008 | A1 |
| 20080021488 | Berberich | Jan 2008 | A1 |
| 20080030170 | Dacquay et al. | Feb 2008 | A1 |
| 20080064925 | Gill et al. | Mar 2008 | A1 |
| 20080064984 | Pflueger | Mar 2008 | A1 |
| 20080071193 | Reuber et al. | Mar 2008 | A1 |
| 20080079391 | Schroeck et al. | Apr 2008 | A1 |
| 20080110261 | Randall et al. | May 2008 | A1 |
| 20080135443 | Frojd et al. | Jun 2008 | A1 |
| 20080146962 | Ritchie et al. | Jun 2008 | A1 |
| 20080146965 | Privitera et al. | Jun 2008 | A1 |
| 20080154151 | Ritchart et al. | Jun 2008 | A1 |
| 20080161682 | Kendrick et al. | Jul 2008 | A1 |
| 20080161718 | Schwindt | Jul 2008 | A1 |
| 20080161719 | Miller et al. | Jul 2008 | A1 |
| 20080161720 | Nicoson et al. | Jul 2008 | A1 |
| 20080183099 | Jorgensen et al. | Jul 2008 | A1 |
| 20080195066 | Speeg et al. | Aug 2008 | A1 |
| 20080200833 | Hardin et al. | Aug 2008 | A1 |
| 20080200836 | Speeg et al. | Aug 2008 | A1 |
| 20080208194 | Bickenbach | Aug 2008 | A1 |
| 20080215056 | Miller et al. | Sep 2008 | A1 |
| 20080221443 | Ritchie et al. | Sep 2008 | A1 |
| 20080221444 | Ritchie et al. | Sep 2008 | A1 |
| 20080221478 | Ritchie et al. | Sep 2008 | A1 |
| 20080221479 | Ritchie et al. | Sep 2008 | A1 |
| 20080221480 | Hibner et al. | Sep 2008 | A1 |
| 20080228104 | Uber et al. | Sep 2008 | A1 |
| 20080232604 | Dufresne et al. | Sep 2008 | A1 |
| 20080234715 | Pesce et al. | Sep 2008 | A1 |
| 20080281225 | Spero et al. | Nov 2008 | A1 |
| 20080287826 | Videbaek et al. | Nov 2008 | A1 |
| 20080306406 | Thompson et al. | Dec 2008 | A1 |
| 20080308607 | Timm et al. | Dec 2008 | A1 |
| 20080319341 | Taylor et al. | Dec 2008 | A1 |
| 20090030405 | Quick et al. | Jan 2009 | A1 |
| 20090062624 | Neville | Mar 2009 | A1 |
| 20090082695 | Whitehead | Mar 2009 | A1 |
| 20090125062 | Arnin | May 2009 | A1 |
| 20090137927 | Miller | May 2009 | A1 |
| 20090171243 | Hibner et al. | Jul 2009 | A1 |
| 20090227893 | Coonahan et al. | Sep 2009 | A1 |
| 20100030020 | Sanders et al. | Feb 2010 | A1 |
| 20100063416 | Cicenas et al. | Mar 2010 | A1 |
| 20100152611 | Parihar et al. | Jun 2010 | A1 |
| 20100160820 | Weikel, Jr. et al. | Jun 2010 | A1 |
| 20100210966 | Videbaek | Aug 2010 | A1 |
| 20100292607 | Moore et al. | Nov 2010 | A1 |
| 20100312140 | Smith et al. | Dec 2010 | A1 |
| 20100317995 | Hibner et al. | Dec 2010 | A1 |
| 20100317997 | Hibner et al. | Dec 2010 | A1 |
| 20100317998 | Hibner et al. | Dec 2010 | A1 |
| 20110152715 | Delap et al. | Jun 2011 | A1 |
| 20110160611 | Ritchart et al. | Jun 2011 | A1 |
| Number | Date | Country |
|---|---|---|
| 3924291 | Jan 1991 | DE |
| 4041614 | Oct 1992 | DE |
| 10034297 | Apr 2001 | DE |
| 10026303 | Feb 2002 | DE |
| 20209525 | Nov 2002 | DE |
| 10235480 | Feb 2004 | DE |
| 0433717 | Jun 1991 | EP |
| 0890339 | Jan 1999 | EP |
| 0995400 | Apr 2000 | EP |
| 1074271 | Feb 2001 | EP |
| 1520518 | Apr 2005 | EP |
| 1579809 | Sep 2005 | EP |
| 1665989 | Jun 2006 | EP |
| 2095772 | Feb 2009 | EP |
| 2106750 | Oct 2009 | EP |
| 1345429 | Dec 1963 | FR |
| 2739293 | Apr 1997 | FR |
| 2018601 | Oct 1979 | GB |
| H10508504 | Aug 1998 | JP |
| 2005530554 | Oct 2005 | JP |
| 2006509545 | Mar 2006 | JP |
| 2006528907 | Dec 2006 | JP |
| 2007502159 | Feb 2007 | JP |
| 9628097 | Sep 1996 | WO |
| 9825522 | Jun 1998 | WO |
| 9831285 | Jul 1998 | WO |
| 9835615 | Aug 1998 | WO |
| 9846290 | Oct 1998 | WO |
| 9933501 | Jul 1999 | WO |
| 0004832 | Feb 2000 | WO |
| 0030546 | Jun 2000 | WO |
| 0059378 | Oct 2000 | WO |
| 0172230 | Oct 2001 | WO |
| 0222023 | Mar 2002 | WO |
| 0232318 | Apr 2002 | WO |
| 02069808 | Sep 2002 | WO |
| 2005013830 | Feb 2005 | WO |
| 2006015302 | Feb 2006 | WO |
| 2007047128 | Apr 2007 | WO |
| 2007095330 | Aug 2007 | WO |
| 2007112751 | Oct 2007 | WO |
| 2008021687 | Feb 2008 | WO |
| 2008040812 | Apr 2008 | WO |
| 2008131362 | Oct 2008 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20100234760 A1 | Sep 2010 | US |
| Number | Date | Country | |
|---|---|---|---|
| 60823038 | Aug 2006 | US |