Abstract: Disclosed are a support body, a body fluid collection set, and a body fluid collection method that can easily support a body fluid collection sheet even by a non-physician. The support body 1 includes a first sheet 10 having an adhesive surface 12 for adhering the body fluid collection sheet 30, and a second sheet 20 adhered to the first sheet 10. The adhesive surface 12 of the first sheet 10 is adhered to the body fluid collection sheet 30 so that the first sheet 10 is separated from the skin 40 and the body fluid collection sheet 30 is peeled off from the skin 40. Thereafter, the second sheet 20 is superposed on the adhesive surface 12, and the body fluid collection sheet 30 is supported on the support body 1.

Abstract: A method for minimally invasive laser ablation of a target tissue within a patient while sparing tissue within a safety zone proximate to the target tissue, comprising: guiding a laser fiber within a patient with a guidance tool; measuring a temperature within the target tissue and the safety zone based on an invasive and a non-invasive thermal sensor; computing a thermal profile in conjunction with a real-time tissue image adapted for guidance of the laser fiber with the guidance tool within the patient; and controlling a laser to deliver energy through the laser fiber, to deliver a minimally therapeutic ablation therapy to the target tissue while ensuring that the safety zone is maintained in a non-ablation condition, based on at least a treatment plan, the measured temperature, and the thermal profile.

Abstract: A bimodal spinneret system including the bimodal spinneret and method for making a surgical buttress having improved characteristics are disclosed. The bimodal spinneret includes at least a distribution of hole diameters to create fibers with a more heterogeneous shear history and die swell. The system and method of using the bimodal spinneret creates a melt blown non-woven fiber mat that is cut into a surgical buttress having unique fabric properties such as differentiated load deflection behavior, flexural stiffness, polymer fiber alignment, fiber crystallinity and subsequent strength retention during in vitro degradation not attainable with unimodal spinneret hole diameters.

Abstract: The present invention is directed to an assembly used in minimally invasive procedures whereby laparoscopic instrument heads, prepositioned in the abdomen of a patient are securely doubly attached and detached internally while under direct laparoscopic visualization. The present invention permits surgeons to utilize full sized laparoscopic instrument heads on needlescopic instrument shafts. Multiple locking structures are employed to securely attach the laparoscopic instrument heads to a needlescopic instrument.

Abstract: A surgical instrument includes a handle assembly, a power source coupled with the handle assembly, and a control circuit coupled with the handle assembly and the power source. The handle assembly, the power source, and the control circuit are configured to drive an end effector of a shaft assembly coupled with the handle assembly to perform an operation on tissue. The control circuit is configured to receive life deduction event data. The control circuit is configured to determine an end of life for the power source based on the life deduction event data.

Abstract: A specimen retrieval system for easier tissue removal during endoscopic surgery. The devices include a specimen tube with a main tube, and a mechanism for pulling and everting the distal end of the tube into the tube, or a side channel provided within the tube. The mechanism may include a tether fixed to the distal edge of the tube, or a grasper operable to grasp the distal edge of the tube.

Abstract: A self-articulating joint is disclosed for a minimally invasive surgical apparatus. The self-articulating joint has a first elbow component pivotably coupled to a second elbow component, wherein the first and second elbow components are biased to form a non-linear angle relative to each other. The self-articulating joint also has an elbow latch configured to releasably hold the first and second elbow components at a substantially fixed non-linear operating angle.

Abstract: An implant having an implant body, a gripper, an elastic pouch, and an elongate member. The pouch can be coupled to the gripper, can have a first part and a second part, can have a contracted state toward which the pouch is elastically biased, and can be reversibly stretchable into a stretched state. The elongate member can have a first end portion coupled to the implant body, a second end portion fastened to the second part of the pouch, and a mid-portion extending (i) from the second end portion, through the pouch to the first part of the pouch, and (ii) out of the pouch to the first end portion. In at least one state of the gripper, the mid-portion can be slidable through the gripper and into the pouch. Other embodiments are also described.

Abstract: In an endoscopic treatment method, a damaged area is formed in at least a portion of a digestive tract along a circumferential direction. The damaged area is formed by performing thermal ablation of mucosal layer and not removing the mucosal layer. An incomplete stenosis is formed in the digestive tract during restoration of the damaged area.

Abstract: A tissue puncture closure device that includes an anchor (208, 508), a sealing pad (210, 510), a compaction member (212, 312, 412, 512), a suture (204, 504), and a suture cutting member (270, 472, 570). The compaction member is configured to compact the sealing pad toward the anchor. The suture is coupled to the sealing pad and anchor, and a portion of the suture extends through at least a portion of the compaction member. The suture cutting member is operable to cut the suture. The suture cutting member is operable within a portion of the compaction member to cut the suture.

Abstract: A deployment instrument for deploying a closure device for sealing a percutaneous puncture in a wall of a body passageway, the deployment instrument including a carrier assembly, wherein the carrier assembly is configured to hold the closure device in a pre-deployment state, and a tensioner assembly, wherein the filament is fixedly attached to the tensioner assembly, wherein the deployment instrument is configured to increase the tension in the filament upon linear movement of the deployment instrument away from the wall of the body passageway when the closure device is anchored to the wall via the anchor such that the tension is gradually increased as the deployment instrument is moved between a first linear distance and a second linear distance greater than the first linear distance from the wall of the body passageway.

Abstract: Disclosed are puncture sealing systems and methods of locating a puncture site within a vessel. The systems can include puncture locating dilators and access sheaths that are configured to locate the puncture site within a vessel so that the position of the puncture site relative to a distal end of the access sheath is known during a puncture sealing procedure.

Abstract: A flexible arm for use in a medical procedure includes a plurality of bushings and a plurality of double-ball members engaged with one another to thereby provide flexibility to the flexible arm. The double-ball members include a concave bore having a convex interior surface. The flexible arm further includes a wire extending through the concave bore of the double-ball members. An exterior diameter of the wire closely approximates or matches an interior diameter of the concave bore at its smallest point such that the curved members are operable to guide the wire as the flexible arm is flexed. The wire may be adjusted to thereby manipulate the amount of engagement between the bushings and the double-ball members to thereby manipulate the flexibility of the flexible arm.

Abstract: A retractor system includes a retractor with an oximeter sensor at its tip and a force sensor coupled to the retractor. The retractor system also includes a system unit which can send signals to and receive signals from the oximeter sensor via optical fibers. The oximeter sensor measures oxygen saturation of a tissue being retracted by the retractor, and the force sensor measures an amount of force that is applied to the retracted tissue by the tip of the retractor. Another retractor system has a closed loop control arrangement with a positioning mechanism which moves the retractor based on measurements of the sensors.

Abstract: A surgical retractor includes a first member defining a longitudinal axis. The first member includes a blade disposed in spaced apart relation relative to the longitudinal axis and a grip surface. A second member has a blade disposed in spaced apart relation relative to the longitudinal axis and a grip surface. The grip surfaces are configured to be drawn together along the longitudinal axis such that the blades are engageable with tissue and connected with the grip surfaces such that the grip surfaces provide a tactile feedback of the tissue engagement. Systems and methods of use are disclosed.

Abstract: A balloon dissector includes a cannula, an expandable bladder, and a cord. The cannula defines a lumen between proximal and distal ends. The expandable bladder is configured to expand when fluid is injected into the lumen and includes an inner surface, a proximal base, and a retainer. The proximal base is selectively coupleable to the distal end of the cannula in a sealing relationship. The retainer is positioned on the inner surface of the expandable bladder. The cord includes a first end, a second end, and a central portion. The one end of the cord extends from the proximal end of the cannula. The cord extends through the lumen of the cannula and through the retainer of the bladder returning into the lumen. The cord configured to draw the expandable bladder into the lumen after the expandable bladder is expanded.

Abstract: A surgical instrument includes a first member having an inner surface and an outer surface. A second member has an inner surface and an outer surface. At least one of the inner surfaces defines at least one mating element and the outer surfaces are engageable with tissue. The members are relatively movable between a first configuration and a second configuration to space the tissue and define an opening between the members. At least one third member defines at least one mating element engageable with the at least one mating element of the inner surface such that the at least one third member is disposed within the opening. Systems and methods are disclosed.

Abstract: An adjustable anchor system provides for securing tissue to bone and includes an anchor with a collapsible suture loop affixed thereto and a tissue suture connected to the collapsible suture loop. After the tissue suture is loaded into the tissue and the anchor implanted into the bone the collapsible loop is collapsed to tension the tissue suture.

Abstract: Assemblies for securing a fractured or weakened bone within a subject's body are provided. The assembly includes a frame having an adjustable flexible member construct thereon. The adjustable flexible member construct is disposed in the frame such that the adjustable flexible member and the frame encircle the fractured or weakened bone.

Abstract: A suturing backstop is disclosed. The suturing backstop has a suturing device receiver configured to receive at least a portion of a tissue bite area of a suturing device. The suturing backstop also has a sewing cuff receptacle. The suturing backstop further has one or more needle guides adjacent the sewing cuff receptacle. The suturing backstop also has one or more alignment stops configured to position said portion of the tissue bite area within the suturing device receiver such that when a needle from the suturing device is extended from a retracted to an engaged position, the needle passes through the sewing cuff receptacle and through a corresponding one of the one or more needle guides. A related method for placing sutures into a sewing cuff of a prosthetic replacement device is also disclosed.

Abstract: An arthroscopic bone channel forming and suturing system useful following formation of a first and a second generally straight channel in a bone, the second channel not intersecting the first channel, the system including a curved bone puncture needle configured to be insertable into the first channel, a curved needle driving assembly configured to manipulate the curved needle to form a curved junction between the first channel and the second channel, a suture snare wire assembly configured to insert a suture snare wire to a suture snare wire pick-up location via the second channel in the bone and a coordinated multi-function driving assembly operative to operate the curved needle driving assembly and the suture snare wire assembly in coordinated operation to cause the suture snare wire to be pulled from the suture pick up location and through the first channel via the junction.

Abstract: Suture delivered patches adapted for interposition, augmentation or repair devices for use in tendon and ligament repair, including rotator cuff repair, have been developed as well as methods for their delivery using suture guided arthroscopic methods. The repair patches may be provided from suitable biocompatible materials. The patches may be delivered using anchored sutures already in use during a surgical repair including, open, minimally invasive, endoscopic, and arthroscopic repair procedures. Additionally, fixation of the suture delivered repair patch is secured along with the normal suture securing workflow of the one or more sutures used to deliver the patch.

Abstract: A suturing kit includes a suture and a suture holder for holding the suture. The suture has a first end and a second, opposite, end. The suture holder includes an elongated wall defining a suture receiving passage that is elongated along a longitudinal axis and terminates at a suture exit opening. The suture receiving passage has a width at least twice the diameter of the suture and receives the suture such that the suture is folded over forming a half loop section spaced from the suture exit opening. A first second of the suture extends from the half loop section toward the first end and a second section of the suture extends from the half loop section towards the second end. The first section and the second section of the suture within the suture receiving passage are aligned parallel to the longitudinal axis.

Abstract: A package for surgical sutures has a base member, an outer wall extending upwardly form the periphery of the base member, a plurality of pyramidal shaped standoff members arranged in an oval shape and a flat suture channel cover member having a plurality of precision holes to lock the cover member to the standoff members of the base member. The inner surface of the outer wall of the base member is a profiled surface and the outer periphery of the cover member has a profiled surface corresponding to the profiled surface of the outer wall of the base member. The profiled surface of the outer wall can consist of a plurality of D shaped vertical members extending from the top surface of the base member to the top of the outer wall.

Abstract: A barbed suture is provided. The barbed suture includes an elongate body and at least one barb extending from the elongate body. The elongate body defines a recess adjacent the at least one barb. Also provided is a method of making a barbed suture. The method includes the steps of providing a suture nest and a punch apparatus configured for operable engagement with the suture nest, loading a suture through the suture nest, engaging the punch apparatus with the suture nest, and disengaging the punch apparatus with the suture nest.

Abstract: A tissue fixation system including a delivery tube and an elongated fastener with a loop at a proximal end and a distal end. A proximal end of an elongated curved needle is attached to the delivery tube. A distal end of the needle is configured to penetrate tissue. The needle includes an open channel sized to receive the elongated fastener with the loop located near the proximal end of the elongated curved needle and the distal end of the elongated fastener located near the distal end of the elongated curved needle. A capture needle is slidably positioned in the delivery tube to slide through the loop in the proximal end of the elongated fastener. The capture needle is configured to grasp the distal end of the elongated fastener and pull the distal end of the elongated fastener through the loop to cinch the elongated fastener.

Abstract: A method for making an expanded, and optionally multi-component and/or colored PTFE monofilament is disclosed. The method includes forming a first paste by mixing a PTFE powder with a hydrocarbon solvent; forming an extrusion preform by pressing the first paste into a form; curing the extrusion preform by exposing the extrusion preform to a first temperature for a first time duration; forming a green monofilament by extruding the first paste through a die; expanding the green monofilament by exposing the green monofilament to a second temperature for a second time duration, the second time duration occurring after the first time duration; stretching the green monofilament substantially along a longitudinal axis of the green monofilament, the stretching the green monofilament occurring after the expanding the green monofilament; and sintering the green monofilament after the stretching the green monofilament.

Abstract: Devices, systems and/or methods for repairing soft tissue adjacent a repair site. In one embodiment, a repair device is delivered with a delivery device system configured to move a cartridge with the repair device disposed therein toward an anvil with soft tissue positioned thereon. The delivery device linearly moves the cartridge toward the anvil with a worm drive positioned within a housing by rotating a thumb wheel disposed around the worm drive. Such linear movement is provided with a finger element extending from the worm drive that is configured to cooperate with an internal surface of the thumb wheel. With this arrangement, upon rotating the thumb wheel, the worm drive rotates with the finger element engaged with the internal surface of the thumb wheel to linearly move the cartridge toward the anvil.

Abstract: A tool assembly for a surgical device includes a first jaw member defining a first tissue contact surface and a second jaw member defining a second tissue contact surface. The first jaw member and the second jaw member are movable in relation to each other between open and closed positions wherein, in the closed position, the first and second tissue contact surfaces are spaced apart from each other and define a tissue gap. A compressible material is secured to a distal end of the first jaw member. The compressible material engages the second jaw member when the first and second jaw members are in the closed position. A surgical device includes the aforementioned tool assembly. A kit includes the compressible material secured on a tool assembly of a surgical device. A method of manufacturing the tool assembly and securing the compressible material is disclosed.

Abstract: A surgical stapling apparatus includes a staple anvil and a staple cartridge having a working surface, one or more rows of individual staple slots formed in the working surface, a knife track formed along a length of the working surface, and a plurality of surgical staples individually disposed within the individual staple slots. The apparatus further includes an actuation sled having a knife and being configured and adapted to movably position the knife axially within the knife track. The apparatus also includes a wound closure material applicator assembly having a needle secured to the knife to dispense a quantity of wound closure material along a length of the knife track as the actuation sled and knife are moved therealong.

Abstract: The present invention discloses a tissue closure device, a tissue closure assembly and a medical instrument. The tissue closure device comprises a base, a pressure plate cooperating with the base, and a staple pushing sheet. The pressure plate is rotatable relatively to the base. The tissue closure device further comprises a staple accommodating portion which is arranged at the distal end of the base and configured to accommodate a closure staple. The staple pushing sheet and the staple accommodating portion are configured to cooperatively drive the closure staple in the staple accommodating portion to deform. In the present invention, a bundled pouch with a gathered center is formed through the tissue closure device, so that risks of stoma fistula arising from subsequent anastomosis through a circular stapler are reduced; and the surgery cost is reduced.

Abstract: A method comprising the steps of obtaining a shaft assembly comprising an end effector, attaching the shaft assembly to a handle of a surgical instrument, wherein the handle comprises a trigger operable to actuate a function of the end effector when the shaft assembly is attached to the handle, removing the shaft assembly from the handle, attaching the shaft assembly to an arm of a surgical robot and removing the shaft assembly from the arm is disclosed.

Abstract: A staple cartridge is disclosed. The staple cartridge can have a longitudinal axis and a cartridge body having a deck, wherein a plurality of staple cavities can be defined in the cartridge body. The staple cavities can be arranged in a plurality of patterns, and the patterns can include a first pattern and a second pattern longitudinally offset from the first pattern. The second pattern can be different than the first pattern. The first pattern can consist of a longitudinally-repetitive pattern of angularly-oriented staple cavities and/or the second pattern can consist of parallel staple cavities.

Abstract: Surgical end effectors having an empty and missing cartridge lockout are disclosed. The surgical end effectors can comprise a first jaw, a second jaw rotatably coupled to the first jaw, and a multi-function firing member configured to translate during a firing stroke, wherein the firing member comprises a notch. The surgical end effectors can also include a lockout spring comprising a hook. The notch in the firing member can be aligned to receive the hook during the firing stroke unless an unfired staple cartridge is positioned in the first jaw. A sled assembly of the unfired staple cartridge can be positioned to deflect the hook out of alignment with the notch.

Abstract: A surgical anchor device for being anchored on the mucous membrane of the inner wall of the intestine, the device having a temporary anchor element presenting anchoring that can be modified in a controlled manner and having a first substantially cylindrical multiply-perforated wall presenting properties of radial elasticity whereby the first wall presents an outer diameter that can be varied in controlled manner, wherein a portion of the inner surface of the first wall is lined with an independent leakproof inner sheath having only its longitudinal ends fastened to the anchor element to define a suction chamber between the inner sheath and the first wall, the temporary anchor element being coupled to a flexible or semi-rigid tube extending outside the anchor element, an open end of the injection-suction tube opening out into the suction chamber enabling air to be injected into or sucked out from the suction chamber.

Abstract: A staple cartridge is disclosed. The staple cartridge can include a cartridge body, a plurality of staples, and an implantable layer. The implantable layer can include an inner portion, an outer portion positioned at least partially around the inner portion, and a plurality of passages formed through the outer portion toward the inner portion. The implantable layer can be porous. An implantable layer can include an outer portion including a plurality of fibers. A method of forming an implantable layer for use with a surgical stapler is also disclosed. The method can include forming at least one passage through an outer surface toward an inner portion of the implantable layer.

Abstract: A surgical stapling assembly comprising a firing member, an end effector, a closure member, and a shaft including an attachment interface is disclosed. The surgical stapling assembly is configured to be attached to a surgical instrument interface by way of the attachment interface. The end effector comprises a first jaw, a second jaw, and a staple cartridge comprising staples configured to be ejected by the firing member. The second jaw is movable relative to the first jaw between an open position, a fully-clamped position, and a collapsed position. The end effector further comprises an interconnection between the first jaw and the second jaw defining a rotational axis about which the second iaw is movable relative to the first iaw. The rotational axis is shiftable toward and away from the first iaw as the second iaw is moved between the open position, the fully-clamped position, and the collapsed position.

Abstract: A surgical instrument assembly comprising a handle, a shaft, and an end effector is disclosed. The end effector comprises a first iaw comprising a tissue-supporting surface defining a plurality of staple cavities defined therein, a second iaw movable relative to the first jaw, a proximal pin coupling the first and second jaws, a first slot configured to receive the proximal pin, a distal pin coupling the jaw and second jaws, and a second slot configured to receive the distal pin. The proximal pin is movable vertically within the first slot. The distal pin is actuatable within the second slot between a first position where the second jaw is in an open position, a second position where the second jaw is in a clamped position, and a third position where the second jaw is in a fully closed position and the second iaw is in contact with the tissue-supporting surface.

Abstract: A surgical fastener applying apparatus including an anvil half-section having a distal end and a longitudinal axis; a cartridge receiving half-section having a distal end and operatively couplable with the anvil half-section such that the distal ends of the half-sections are in juxtaposed relation; and a deflection control system operatively engaged with and reinforcing the distal end of the anvil half-section when a force is applied to the distal end of the anvil half-section in a direction transverse to the longitudinal axis.

Abstract: The problem of attaching a donor nerve stump to a recipient nerve for an end-to-side coaptation is solved by the use of a tissue connector. The tissue connector can have a body for receiving the donor nerve stump and one or more overflaps for attaching the tissue connector with the donor nerve stump therein to the epineurium on the side of the recipient nerve. Sutures can also be used to secure the tissue connector and nerves in place.

Abstract: A surgical instrument includes a stapling head assembly and a first locking feature. The stapling head assembly has a cartridge housing, a staple deck, a plurality of staples, a staple driver, a cylindraceous knife, and a trocar. The cartridge housing extends along a longitudinal axis that is configured to removably couple with a portion of a shaft assembly. The staple driver is configured to translate distally from a proximal driver position toward a distal driver position to thereby drive each of the plurality of staples distally from an annular array of staple pockets, respectively, for forming the plurality of staples in a tissue of a patient. The first locking feature is operatively connected to the cartridge housing and configured to removably couple against the portion of the shaft assembly for selectively coupling and decoupling the stapling head assembly relative to the portion of the shaft assembly.

Abstract: A surgical instrument includes a handle assembly and an adapter assembly. The handle assembly includes a handle housing and a processor disposed within the handle housing. The adapter assembly includes a knob housing, an elongate body, a plurality of electrical components, and a flex circuit. The knob housing is configured to be connected to the handle housing. The elongate body extends distally from the knob housing and has a distal end configured to be coupled to an end effector. The electrical components are disposed within the elongate body. The flex circuit has a proximal end configured to be electrically connected to the processor, and a distal end configured to be electrically connected to the electrical components.

Abstract: An apparatus includes a body assembly, an end effector, and a firing assembly. The body includes a handle portion and a shaft portion. The end effector includes a staple driver. The firing assembly includes a driver actuator and a trigger. The driver actuator is configured to actuate the staple driver. The driver actuator is slidably housed within the shaft portion. The trigger includes a lever and an integral spring member. The lever is pivotally coupled to the handle portion via a pivot boss of the handle portion. The trigger is configured to pivot between a first position and a second position to slide the driver actuator within the shaft portion, to thereby actuate the staple driver. The integral spring member is at least partially housed within a spring channel of the handle portion and is configured to resiliently bias the trigger toward the first position.

Abstract: Systems, methods, and devices for the treatment of acute ischemic stroke that provide immediate blood flow restoration to a vessel occluded by a clot and, after reestablishing blood flow, address the clot itself Immediate blood flow restoration advantageously can facilitate natural lysis of the clot and also can reduce or obviate the concern for distal embolization due to fragmentation of the clot. Several embodiments of the invention provide for progressive, or modular, treatment based upon the nature of the clot. For example, the progressive treatment can include immediate restoration of blood flow, in-situ clot management, and/or clot removal depending on the particular circumstances of the treatment. The in-situ clot management can include, for example, lysis, maceration, and/or removal.

Abstract: A method of providing retrograde perfusion of a patient's brain includes occluding a jugular vein of a subject at a jugular occlusion location, and passively shunting arterial blood from an artery of the subject to a location in the jugular vein distal to the jugular occlusion location.

Abstract: An occlusive medical device system may include an elongate shaft having a distal strain relief portion and a lumen extending longitudinally through the elongate shaft, the elongate shaft including a plurality of retaining arms extending distally from the distal strain relief portion; an occlusive medical device including a proximal mounting portion fixed to an expandable occlusive element; and a release wire disposed within the lumen of the elongate shaft. The plurality of retaining arms may extend into the proximal mounting portion. The release wire may be configured to engage the plurality of retaining arms in a distal engagement position, thereby urging the plurality of retaining arms radially outward into releasable engagement with the proximal mounting portion. When the release wire is in a proximal released position, the plurality of retaining arms is deflectable radially inward to disengage from the proximal mounting portion.

Abstract: A handle assembly for use with a surgical instrument including a housing, a movable handle, a plunger, a first linkage, and a second linkage. The movable handle is pivotably mounted to the housing about a handle pin. The plunger is disposed at least partially within the housing. Distal translation of the plunger relative to the housing is configured to affect a function of the surgical instrument. The first linkage is disposed at least partially within the housing. A first portion of the first linkage is pivotable about the housing, and a second portion of the first linkage is slidable relative to the handle pin. The second linkage is disposed at least partially within the housing. A first portion of the second linkage is pivotable about the plunger, and a second portion of the second linkage is pivotable about a third portion of the first linkage.

Abstract: A tissue clipping apparatus, comprises a flexible, elongate member, a proximal end of which remains external to the body accessible to a user while a distal end of the flexible member is inserted into the body to a location adjacent to target tissue to be clipped and a control wire extending through the flexible member in combination with a capsule releasably coupled to a distal end of the flexible member and a clip a proximal portion of which is received within the capsule. A joint releasably coupling the clip to the control wire, includes a yoke extending around a proximal end of the clip and a frangible link which fails when subject to a predetermined force to separate the clip from the control wire.

Abstract: A resection guide system for resecting an end of bone includes an anchoring block having an elongate shaft and an opening extending through the anchoring block at one end thereof. The opening is sized to receive a rod therein and defines an axis. A translation member includes a housing and a shaft extending therefrom. The housing is engageable to the shaft of the anchoring block in a first configuration in which the shaft of the translation member is oriented at a first angle relative to the axis of the opening and a second configuration in which the shaft of the translation member is oriented at a second angle relative to the axis of the opening. A resection guide assembly connects to the shaft of the translation member and has a resection guide surface adapted to guide a cutting instrument along a plane defined by the resection guide surface.

Abstract: A surgical tool with a housing, and a cutter support shaft operably connected to a motor to effect rotation of the shaft with a drive transmission configured between the motor and the shaft to effect oscillating rotary movement of the shaft and cutter is disclosed.