Brachytherapy clip and applicator

Information

  • Patent Grant
  • 11660469
  • Patent Number
    11,660,469
  • Date Filed
    Thursday, January 7, 2021
    3 years ago
  • Date Issued
    Tuesday, May 30, 2023
    a year ago
Abstract
A surgical implant includes a biocompatible member configured for securement to an underlying target surgical site and a radiation source integrated into or onto the biocompatible member. The surgical implant may be one of a clip, pin, or coil and the radiation source includes at least one brachytherapy capsule, or other radioactive material incorporated therein or provided thereon. The radioactive material provides a dose of radiation to the target surgical site. The surgical implant may also be formed from titanium, stainless steel or polymers. A surgical applier is provided for allowing a surgeon to apply the implant to a patient's tissue.
Description
BACKGROUND
1. Technical Field

The present disclosure relates to surgical implants, clips or fasteners and, more particularly, to surgical low dose brachytherapy implants, clips or fasteners and applicators therefor.


2. Background of Related Art

Generally, brachytherapy is an advanced form of cancer treatment. Specifically, permanent radioactive seeds, sutures, buttresses or the like are placed in or near the cancer site itself, which radioactive seeds, sutures or buttresses emit a relatively low dose of radiation directly to the cancer site while reducing exposure of surrounding healthy tissue to the radiation.


Depending on the underlying cancer to be treated and on the underlying tissue, particular dosimetry guidelines have been developed for the placement of radioactive seeds, sutures or buttresses and for the radiation levels emitted by the radioactive seeds, sutures or buttresses. Generally, the placement of such radioactive seeds, sutures or buttresses are at predefined distances relative to one another in order to enable effective dosimetry. The radioactive sutures and/or buttresses generally include radioactive seeds incorporated therein, which have been placed at fixed, uniform distances to one another.


In view thereof, a need exists, and it is desirous, for surgical brachytherapy implants, clips or fasteners, which may be placed at any desired location relative to the target cancer site. The need also exists, and it is desirous, for an apparatus capable of placing, individually, the surgical brachytherapy implants, clips or fasteners. The brachytherapy implant can be configured as a staple, clip, pin, tack, coil or other implant, to name a few.


The need also exists, and it is desirous, for methods of using the surgical brachytherapy implants, clips or fasteners, and/or the apparatus for placing, individually, the surgical brachytherapy implants, clips or fasteners.


SUMMARY

The present disclosure relates to surgical implants, clips, and/or fasteners.


According to an aspect of the present disclosure, a surgical implant is provided comprising a biocompatible member configured for securement to an underlying target surgical site and a radiation source integrated into or onto the biocompatible member.


The surgical implant may be one of a clip, pin, or coil and the radiation source includes at least one brachytherapy capsule providing a dose of radiation to the target surgical site. The surgical implant may also be formed from titanium, stainless steel or polymers.


According to another aspect of the present disclosure, the clip comprises a deformable backspan, wherein a first leg extends from a first end of the backspan and a second leg extends from a second end of the backspan, and wherein the first leg and the second leg extend substantially in the same direction from the backspan.


A biocompatible radioactive material may be dispersed throughout the surgical implant such that the entirety of the surgical implant irradiates radioactively. The surgical implant may also be coated with one of gold or a colored oxide layer such that the surgical implant is substantially visible in the surgical field during an open procedure or radiographic location.


According to another aspect of the present disclosure, the pin comprises a leg having a proximal end and a distal end and a head extending from the proximal end of the leg at an angular orientation relative to a longitudinal axis of the leg. The pin may include a barb extending from the distal end of the leg and may further include a barb extending from a free end of the head.


According to still another aspect of the present disclosure, the coil comprises a body portion having a first end and a second end opposite the first end, the first end of the body portion having a sharp tissue penetrating point, and the second end having a tang disposed generally inward toward the center of the body portion. The body portion may include approximately 2.5 coils.


According to yet another aspect of the present disclosure, a method of performing a surgical procedure at a target surgical site may be provided. The method may comprise providing a surgical applier loaded with at least one surgical implant, wherein the at least one surgical implant includes a biocompatible member configured for securement to an underlying target surgical site and a radiation source integrated into or onto the biocompatible member, placing the surgical applier adjacent to a first location of the target surgical site, and firing the surgical applier to secure a first surgical implant of the at least one surgical implant to the first location of the target surgical site.


The method may further comprise relocating the surgical applier to a second location of the target surgical site and re-firing the surgical applier to secure a second surgical implant of the at least one surgical implant to the second location of the target surgical site.


The method may further include relocating the surgical applier at a plurality of locations of the target surgical site and re-firing the surgical applier to secure a surgical implant of the at least one surgical implant to each respective location of the plurality of locations of the target surgical site. Additionally, the method may further include relocating the surgical applier at the plurality of locations of the target surgical site and arranging the at least one surgical implant in any configuration, in any pattern, or in any quantity.


A surgical implant of the at least one surgical implant in the form of one of a clip, pin, or coil may also be provided wherein the radiation source is at least one brachytherapy capsule providing a dose of radiation to the target surgical site. A surgical implant of the at least one surgical implant may also be provided wherein a biocompatible radioactive material is dispersed throughout the surgical implant such that the entirety of the surgical implant irradiates radioactively.


According to still another aspect of the present disclosure, a surgical applier is provided. The surgical applier may comprise a handle assembly and an endoscopic shaft assembly rotatably supported on and extending from the handle assembly, the endoscopic shaft assembly configured to articulate off-axis, the endoscopic shaft assembly including an end effector supported at a distal end of the endoscopic shaft assembly, and a plurality of surgical implants loaded therein, wherein a distal-most surgical implant of the plurality of implants is disposable in the end effector and is fired by the end effector upon an actuation of the handle assembly, each surgical implant includes a biocompatible member configured for securement to an underlying target surgical site, and a radiation source integrated into or onto the biocompatible member.


The surgical applier may further comprise a cartridge loaded with the plurality of surgical implants wherein the endoscopic shaft assembly is configured to selectively receive the cartridge. The plurality of surgical implants may be one of a clip, pin, or coil and the radiation source is at least one brachytherapy capsule providing a dose of radiation to the target surgical site.





BRIEF DESCRIPTION OF THE DRAWINGS

The present disclosure will be further described with reference to the accompanying drawings, wherein like reference numerals refer to like parts in the several views, and wherein:



FIGS. 1-5 are plans views of various surgical implants in accordance with embodiments of the present disclosure;



FIG. 6 is a plan view of another embodiment of a surgical implant in accordance with the present disclosure;



FIGS. 7 and 8 are perspective views of yet another embodiment of a surgical implant in accordance with the present disclosure;



FIG. 9 is a perspective view of a surgical applying apparatus according to an embodiment of the present disclosure, for applying the surgical implants of FIGS. 1-5; and



FIG. 10 is a perspective view of a surgical applying apparatus according to another embodiment of the present disclosure, for applying the surgical implants of FIGS. 7 and 8.





DETAILED DESCRIPTION OF EMBODIMENTS

Embodiments of the presently disclosed surgical applying apparatus, and surgical marker or implant, will now be described in detail with reference to the drawings, in which like reference numerals designate identical or corresponding elements in each of the several views. In the drawings and in the description that follows, the term “proximal” will refer to the end of the applying apparatus which is closest to the operator, while the term “distal” will refer to the end of the applying apparatus which is farthest from the operator.


In accordance with the present disclosure, as illustrated in FIGS. 1-5, a surgical implant or clip 100 is provided and includes a backspan or crown 102, a first leg 104 extending from a first end of backspan 102, and a second leg 106 extending from a second end of backspan 102. The first leg 104 and the second leg 106 may extend in the same direction from backspan 102.


Surgical clip 100 may have an unformed condition wherein the first leg 104 and the second leg 106 are parallel, or substantially parallel, to one another and spaced a relative distance from one another. Surgical clip 100 may have a formed condition wherein the first leg 104 and the second leg 106 are parallel, or substantially parallel, to one another and in relative close proximity to one another. In embodiments, first leg 104 and second leg 106 are substantially out of parallel relative to one another.


Surgical clip 100 may be fabricated from a formable material, such as, for example, titanium, stainless steel or polymers. In this manner, surgical clip 100 may be introduced over a target vessel or tissue while in an unformed condition, and then formed or fastened onto the target vessel or tissue to secure the surgical clip 100 to the target vessel or tissue. It is contemplated that surgical clips 100 may be fabricated from any non-degradable, biocompatible material known by those having skill in the art.


In accordance with the present disclosure, as illustrated in FIG. 1, surgical clip 100 may include a brachytherapy capsule or seed 110, or the like, integrated into backspan 102 thereof. It is contemplated, as illustrated in FIG. 2, that multiple brachytherapy capsules 110 may be integrated into backspan 102 of surgical clip 100. It is further contemplated, as illustrated in FIGS. 3 and 4, that at least one brachytherapy capsule 110 may be secured to an outer surface (e.g., distal, proximal or side) of backspan 102 of surgical clip 100.


Also in accordance with the present disclosure, as illustrated in FIGS. 2, 3 and 4, surgical clip 100 may include a brachytherapy capsule 110, or the like, integrated into first leg 104 and/or second leg 106 thereof. It is contemplated that multiple brachytherapy capsules 110 may be integrated into first leg 104 and/or second leg 106 of surgical clip 100. It is further contemplated that at least one brachytherapy capsule 110 may be secured to an outer surface (e.g., inboard, outboard or side) of first leg 104 and/or second leg 106 of surgical clip 100.


Any other combinations of placement of brachytherapy capsules 110 along or integration of brachytherapy capsules 110 in surgical clip 100 is contemplated and within the scope of the present disclosure.


Each brachytherapy capsule 100 may include a radioactive material disposed in a shell, or a radioactive material disposed on or throughout a solid body, wherein the radioactive material includes any of a number of radioactive isotopes. Possible low dose isotopes include, but are not limited to, Cesium-131 (131Cs), Iridium-192 (192Ir), Iodine-125 (125I), Palladium-103 (103Pd), and Ytterbium-169 (169Yb). Therapeutic dosages may range from 80 to 150 Gy depending on the isotope and desired exposure. Surgical clip 100 may have various target energies to provide flexibility in dosimetry planning.


It is envisioned that brachytherapy capsules 100 constitute a radiation source and may be dimensioned so as to produce a particular strength of radiation field therefrom, and/or a particular geometry of the radiation field therefrom.


It is further envisioned, as illustrated in FIG. 5, that surgical clip 100 may be processed such that the entirety of surgical clip irradiates radioactively from radioactive material 120 dispersed throughout surgical clip 100. For example, and within the purview of the present disclosure, surgical clip 100 may be processed so as to provide a known degree of radiation field strength. Specifically, in an embodiment, surgical clip 100 may be a polymeric surgical clip fabricated from a radioactive biocompatible material.


In an embodiment, surgical clips 100 are constructed to be visible in the surgical field during either an open or a laparoscopic procedure. Surgical clips 100 may be coated with a material, such as, for example, gold, or coated with a colored oxide layer to make surgical clips 100 relatively more visible. Gold coatings or other coatings may be utilized to enable radiographic location of surgical clips 100 during follow-up procedures. In this manner, surgical clips 100 may serve as fiduciary markers.


In accordance with the present disclosure, by fastening the surgical clip 100 onto a target vessel or tissue, a therapeutic dose of radiation can be applied to a set location and known volume of tissue based on the activity and isotope material of the brachytherapy capsule 110.


Surgical clips 100 serve the purpose of applying a local therapeutic dose of radiation to, for example, a tumor or to a resection site after removal of a cancerous tumor. Surgical clips only require sufficient mechanical strength to hold brachytherapy capsule 110 in place and are not intended to hold tissue structures together.


Surgical clips 100 may be applied or fastened to any number of tissues having a tumorous growth, such as, for example lung tissue, solid organs, gastro-intestinal tissue, and soft tissues.


In accordance with the present disclosure, it is envisioned that surgical clips 100 may be applied separately, and individually, at a location of choice by the attending clinician. Since brachytherapy capsule 110 has a set three-dimensional field of known radiation strength and geometry, multiple individual surgical clips 100 may be applied to the target tissue to enable effective dosimetry.


It is contemplated that surgical clips 100 may be applied or arranged in any configuration, pattern, or quantity to achieve the intended purpose. For example, surgical clips 100 may be arranged in, for example, a straight line, arcuate, triangular, rectangular, circular or other configuration. It is further contemplated that surgical clips 100 may be fastened to the target tissue a uniform distance from one another, various distances from one another, or a combination thereof.


In certain instances, uniform and accurate spacing of surgical clips 100 is desired. For example, if spacing between adjacent surgical clips 100 is not accurate then the desired dosimetry may not be achieved.


In accordance with the present disclosure, while a surgical implant, in the form of a clip 100 has been shown and described in detail, it is contemplated that the surgical implant may include, and is not limited to, a surgical pin, a surgical tack, a surgical coil or the like. As mentioned above, and as contemplated herein, any of the surgical implants may be fabricated from a biocompatible material, such as, for example, titanium, stainless steel or polymers. Likewise, as mentioned above, and as contemplated herein, any of the surgical implants may incorporate therein or support thereon a brachytherapy capsule 110, or may be processed such that the entirety of surgical implant irradiates radioactively.


For example, with reference to FIG. 6, a surgical implant in the form of a surgical pin is shown and generally designated as 200. Surgical pin 200 may include a leg 204 having a proximal end 204a (not shown) and a distal end 204b (not shown), and a head or arm 202 extending from proximal end 204a. Head 202 may extend orthogonally from a longitudinal axis of leg 204 or at any desired angular orientation relative to the longitudinal axis of leg 204. It is contemplated that surgical pin 200 may include a barb 206 or the like projecting from distal end 204b of leg 204. It is further contemplated that surgical pin 200 may include a barb or tang 208 projecting distally from a free end of head or arm 202, wherein tang 208 functions to help fix an orientation of surgical pin 200 in the target tissue following implantation.


In accordance with the present disclosure, at least one brachytherapy capsule 110 may be disposed within or onto head 202 of surgical pin 200, or may be disposed within or onto leg 204 of surgical pin 200. It is further envisioned that surgical pin 200 may be processed such that the entirety of surgical pin irradiates radioactively from radioactive material dispersed throughout surgical pin 200. For example, and within the purview of the present disclosure, surgical pin 200 may be processed so as to provide a known degree of radiation field strength.


Surgical pin 200 may be fabricated from, for example, titanium, stainless steel or polymers. In an embodiment, surgical pin 200 may be a polymeric surgical pin fabricated from a radioactive biocompatible material. Some examples of non-degradable biocompatible polymers include polyolefins such as polyethylenes and polypropylenes, nylons, polyesters, silicones, polyimides, polymethylmethacrylates, polyurethanes, PTFE, polyethersulfone, polysulfone, PEEK, to name a few.


As an additional example, with reference to FIGS. 7 and 8, a surgical implant in the form of a surgical tack or coil is shown and generally designated as 300. Specifically, surgical tack 300 is a helical-shaped coil fastener. Surgical tack 300 is designed for application to tissue by rotating surgical tack 300 into and through the target tissue. Surgical tack 300 generally includes a coil body portion 302, having approximately 2½ coils and terminating in a sharp tissue penetrating point 304. Surgical tack 300 includes a tang 306 at an opposite end of coil body portion 302 from penetrating point 304. Tang 306 extends generally inwardly toward the center of coil body portion 302.


In accordance with the present disclosure, at least one brachytherapy capsule 110 may be disposed within or onto tang 306 of surgical tack 300, or may be disposed within or onto coil body portion 302 of surgical tack 300. It is further envisioned that surgical tack 300 may be processed such that the entirety of surgical tack irradiates radioactively from radioactive material dispersed throughout surgical tack 300. For example, and within the purview of the present disclosure, surgical tack 300 may be processed so as to provide a known degree of radiation field strength.


Surgical tack 300 may be fabricated from, for example, titanium, stainless steel or polymers. In an embodiment, surgical tack 300 may be a polymeric surgical coil fabricated from a radioactive biocompatible material.


While surgical implants in the form of clips, pins and coils have been illustrated and described herein, it is within the scope of the present disclosure that the surgical implants may also include two-part fasteners, tacks, locking hinged fasteners, staples or the like.


In order to place surgical clips 100 disclosed herein, in accordance with the present disclosure, as illustrated in FIG. 9, a surgical applier 400 is provided. Surgical applier 400 includes a handle assembly 410, and an endoscopic shaft assembly 420 extending from handle assembly 410. Endoscopic shaft assembly 420 is rotatably connected to handle assembly 410 such that endoscopic shaft assembly 420 is rotatable about a longitudinal axis “X1-X1” thereof. Endoscopic shaft assembly 420 may include a proximal portion 422, and a distal portion 424 pivotably connected to proximal portion 422, wherein distal portion 424 may be articulated relative to proximal portion 422.


Distal portion 424 of endoscopic shaft assembly 420 may include a quantity of surgical clips 100 (not shown) pre-loaded therein, or may be configured to selectively receive a cartridge assembly (not shown) which is loaded with a quantity of surgical clips 100 therein. For example, the cartridge assembly may be loaded with ten or fewer surgical clips 100, or any quantity of surgical clips 100.


Distal portion 424 of endoscopic shaft assembly 420 may include a firing and forming mechanism configured to load a single (e.g., distal-most) surgical clip 100 into a pair of jaws 430, and to form the surgical clip 100 loaded into the pair of jaws 430. Surgical applier 400 is configured to fire and form a single surgical clip 100 during a complete firing sequence.


For a more detailed description of the construction and operation of an example of a surgical applier 400, reference may be made to U.S. Pat. No. 8,403,946, the entire content of which is incorporated herein by reference.


In order to place surgical tacks 300, in accordance with the present disclosure, a tack applier 500 (FIG. 10) may be provided which is either pre-loaded with surgical tacks 300, or which may selectively receive a cartridge loaded with surgical tacks 300. The tack applier 500 may be configured to fire or deliver a single surgical tack 300 during a full firing sequence. The tack applier 500 may also be configured to articulate in order to facilitate the firing of surgical tacks 300 therefrom.


For a more detailed description of the construction and operation of an example of a surgical tack applier 500 capable of firing surgical tacks 300, reference may be made to U.S. Pat. No. 5,830,221, the entire content of which is incorporated herein by reference.


In accordance with the present disclosure, the combination of surgical implants and appliers disclosed herein provides the clinician a relatively great deal of flexibility and customization in placing radiation emitting implants (e.g., surgical clips 100, surgical pins 200, surgical tacks 300, etc.) at desired target surgical sites, whereby the applier (e.g., surgical applier 400) is articulatable and/or rotatable to provide the clinician with increased flexibility and precision in placing the radiation emitting implants.


It is contemplated for example, that a geometry of surgical clip 100, surgical pin 200 and surgical tack 300; and a geometry of a tip (e.g., the pair of jaws, etc.) of a surgical applier may be optimized to work together as location guides to optimally place surgical clip 100, surgical pin 200 and/or surgical tack 300 adjacent to one another, wherein the brachytherapy capsule 100 has a known geometry and radiation field strength, to achieve effective dosimetry.


In accordance with the present disclosure, the location of placement of surgical clips 100, surgical pins 200 and/or surgical tacks 300 is not limited to a predefined geometry, pattern, density, or the like. In particular, as mentioned above, surgical clips 100, surgical pins 200 and/or surgical tacks 300 may be fastened to a target tissue site in any geometry, pattern and/or density, as the clinician desires or needs.


By way of example, the ability to fasten surgical clips 100, surgical pins 200 and/or surgical tacks 300, to a target tissue site (e.g., lung tissue in a lung resection procedure), in any geometry, pattern and/or density, may be quite useful in a lung cancer patient, where many lung cancer patients suffer from impaired lung volume and cannot tolerate unnecessary loss of lung volume, and may need multiple rows of brachytherapy sources to ensure treatment of an inadequately narrow surgical margin.


In any of the embodiments disclosed herein, the surgical implants (e.g., surgical clips 100, surgical pins 200 and/or surgical tacks 300) may be incorporated into, or configured for use with, devices that are part of a powered surgical system or robotic surgical system.


It will be understood that various modifications may be made to the embodiments disclosed herein. Therefore, the above description should not be construed as limiting, but merely as exemplifications of preferred embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended thereto.

Claims
  • 1. A surgical implant comprising: a backspan including a first end and a second end, the backspan including an inner surface configured to face tissue and an opposing outer surface, wherein the backspan is substantially v-shaped and includes first and second segments extending from the respective first and second ends of the backspan to an apex;a first leg extending from the first end of the backspan;a second leg extending from the second end of the backspan in the same direction as the first leg;at least one first brachytherapy capsule of a plurality of first brachytherapy capsules integrated into and embedded partially and transversely within the inner surface of the backspan at the apex, wherein the plurality of first brachytherapy capsules are interspaced from each other and integrated into the backspan; anda second brachytherapy capsule integrated into the first leg or the second leg in interspaced relation relative to the at least one first brachytherapy capsule.
  • 2. The surgical implant according to claim 1, wherein the second brachytherapy capsule is one of a plurality of second brachytherapy capsules integrated into the first leg or the second leg, the plurality of second brachytherapy capsules disposed in interspaced relation relative to each other.
  • 3. The surgical implant according to claim 2, wherein the plurality of second brachytherapy capsules are integrated into both the first and second legs.
  • 4. The surgical implant according to claim 2, wherein the plurality of second brachytherapy capsules are integrated into the inner surface of the first leg or the inner surface of second leg.
  • 5. The surgical implant according to claim 1, further comprising a brachytherapy capsule secured to the outer surface of the backspan.
  • 6. The surgical implant according to claim 1, wherein each of the first and second legs includes an inner surface configured to face the tissue and an opposing outer surface, and the second brachytherapy capsule is integrated into and embedded partially and transversely within the inner surface of the first leg or the second leg.
  • 7. The surgical implant according to claim 6, further comprising a brachytherapy capsule secured to an outer surface of the first leg or the second leg.
  • 8. The surgical implant according to claim 1, further comprising a coating of a colored oxide or gold.
  • 9. The A surgical applier comprising: a handle assembly; andan endoscopic shaft assembly extending from the handle assembly, the endoscopic shaft assembly including a distal portion having a surgical implant loaded therein, the surgical implant including: a backspan including a first end and a second end, the backspan including an inner surface configured to face tissue and an opposing outer surface;wherein the backspan is substantially v-shaped and includes first and second segments extending from the respective first and second ends of the backspan to an apex;a first leg extending from the first end of the backspan;a second leg extending from the second end of the backspan in the same direction as the first leg;at least one first brachytherapy capsule of a plurality of first brachytherapy capsules integrated into and embedded partially and transversely within the inner surface of the backspan at the apex;wherein the plurality of first brachytherapy capsules are interspaced from each other and integrated into the backspan; anda second brachytherapy capsule integrated into the first leg or the second leg in interspaced relation relative to the at least one first brachytherapy capsule.
  • 10. The A method of performing a surgical procedure comprising: placing a distal portion of an endoscopic shaft assembly of a surgical applier adjacent to tissue at a surgical site, the distal portion of the endoscopic shaft assembly having a surgical implant loaded therein, the surgical implant including:a backspan including a first end and a second end, the backspan including an inner surface configured to face the tissue and an opposing outer surface, wherein the backspan is substantially v-shaped and includes first and second segments extending from the respective first and second ends of the backspan to an apex;a first leg extending from the first end of the backspan;a second leg extending from the second end of the backspan in the same direction as the first leg;at least one first brachytherapy capsule of a plurality of first brachytherapy capsules integrated into and embedded partially and transversely within the inner surface of the backspan at the apex, wherein the plurality of first brachytherapy capsules are interspaced from each other and integrated into the backspan; anda second brachytherapy capsule integrated into the first leg or the second leg in interspaced relation relative to the at least one first brachytherapy capsule; andfiring the surgical applier to secure the surgical implant to the tissue.
CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a Divisional Application claiming the benefit of and priority to U.S. patent application Ser. No. 16/227,713, filed Dec. 20, 2018, which is a Continuation Application claiming the benefit of and priority to U.S. patent application Ser. No. 14/989,406, filed Jan. 6, 2016, now U.S. Pat. No. 10,159,850, the entire content of each of which is hereby incorporated by reference herein.

US Referenced Citations (84)
Number Name Date Kind
4754745 Horowitz Jul 1988 A
5030195 Nardi Jul 1991 A
5460592 Langton et al. Oct 1995 A
5626592 Phillips et al. May 1997 A
5713911 Racenet et al. Feb 1998 A
5830221 Stein et al. Nov 1998 A
5906573 Aretz May 1999 A
6030333 Sioshansi et al. Feb 2000 A
6146322 Papirov et al. Nov 2000 A
6264596 Weadock Jul 2001 B1
6293899 Sioshansi Sep 2001 B1
6309339 Ciezki Oct 2001 B1
6425903 Voegele Jul 2002 B1
6471630 Sioshansi et al. Oct 2002 B1
6547812 Hu Apr 2003 B1
6575887 Schrayer Jun 2003 B1
6575888 Zamora et al. Jun 2003 B2
6589502 Coniglione et al. Jul 2003 B1
6599230 Hastings et al. Jul 2003 B2
6616592 Rosenthal et al. Sep 2003 B1
6629988 Weadock Oct 2003 B2
6749553 Brauckman et al. Jun 2004 B2
6761680 Terwilliger et al. Jul 2004 B2
6773390 McDaniel Aug 2004 B2
6786858 Terwilliger et al. Sep 2004 B2
6820318 Terwilliger et al. Nov 2004 B2
6926733 Stinson Aug 2005 B2
6969344 Drobnik et al. Nov 2005 B2
6997862 Terwilliger et al. Feb 2006 B2
7008368 Terwilliger et al. Mar 2006 B2
7060020 Terwilliger et al. Jun 2006 B2
7070554 White et al. Jul 2006 B2
7105018 Yip et al. Sep 2006 B1
7942931 Gonzalez et al. May 2011 B2
7972260 Wazer et al. Jul 2011 B2
8061520 Stopek Nov 2011 B2
8069980 Stopek et al. Dec 2011 B2
8267849 Wazer et al. Sep 2012 B2
8292068 Stopek et al. Oct 2012 B2
8342376 Surti Jan 2013 B2
8403946 Whitfield et al. Mar 2013 B2
8454489 Drobnik et al. Jun 2013 B2
8486047 Stopek Jul 2013 B2
8529819 Ostapoff et al. Sep 2013 B2
8551132 Eskridge et al. Oct 2013 B2
8579785 Shariati Nov 2013 B2
8939153 Reicher Jan 2015 B1
9198654 Reicher Dec 2015 B1
10159850 Racenet et al. Dec 2018 B2
10926105 Racenet et al. Feb 2021 B2
20020010480 Sancoff et al. Jan 2002 A1
20020058057 Kaplan May 2002 A1
20040006372 Racenet Jan 2004 A1
20040068157 Gellman Apr 2004 A1
20040109823 Kaplan Jun 2004 A1
20040192998 Brauckman Sep 2004 A1
20050027156 Pulido Feb 2005 A1
20070021643 Lamoureux Jan 2007 A1
20070055144 Neustadter Mar 2007 A1
20070106108 Hermann May 2007 A1
20070244351 Wazer et al. Oct 2007 A1
20080045773 Popowski Feb 2008 A1
20090012347 Helle et al. Jan 2009 A1
20090018535 Schechter et al. Jan 2009 A1
20090030260 Mick Jan 2009 A1
20090131734 Neustadter May 2009 A1
20100191262 Harris et al. Jul 2010 A1
20100254897 Frank Oct 2010 A1
20110152839 Cima et al. Jun 2011 A1
20110245578 Wazer et al. Oct 2011 A1
20120029533 Whitfield Feb 2012 A1
20120059394 Brenner et al. Mar 2012 A1
20120125792 Cassivi May 2012 A1
20130068815 Bruewer Mar 2013 A1
20130087603 Viola Apr 2013 A1
20130178910 Azamian Jul 2013 A1
20140066688 Cassivi Mar 2014 A1
20140332581 Dudai Nov 2014 A1
20140378739 Munro, III et al. Dec 2014 A1
20150031935 Wazer Jan 2015 A1
20150129633 Shariati May 2015 A1
20150375011 Spittle et al. Dec 2015 A1
20170246476 Munro, III Aug 2017 A1
20210024360 Yamazaki et al. Jan 2021 A1
Foreign Referenced Citations (2)
Number Date Country
1126900 Aug 2001 EP
02091928 Nov 2002 WO
Non-Patent Literature Citations (4)
Entry
Japanese Notice of Allowance corresponding to counterpart Patent Application No. JP 2016-252879 dated Jul. 6, 2021.
Extended European Search Report for EP 17 15 0346 dated Jul. 13, 2017.
Partial European Search Report issued in corresponding Application No. EP17150346, dated Mar. 29, 2017, 7 pages.
Japanese Office Action dated Jul. 14, 2020 corresponding to counterpart Patent Application JP 2016-252879.
Related Publications (1)
Number Date Country
20210146154 A1 May 2021 US
Divisions (1)
Number Date Country
Parent 16227713 Dec 2018 US
Child 17143194 US
Continuations (1)
Number Date Country
Parent 14989406 Jan 2016 US
Child 16227713 US