Abstract: Systems and methods are provided for adjusting a field of view of a medical imaging system, such as for an ultrasound imaging system. A system (e.g., an ultrasound imaging system) is provided herein that includes a matrix array probe. The matrix array probe includes a plurality of transducer elements arranged in an array with an elevation direction and an azimuth direction. The system includes a controller circuit that is configured to control the matrix array probe to acquire ultrasound data from a sector field of view (FOV) with a subset of the plurality of transducer elements. The sector FOV having a virtual apex. The controller circuit is further configured to shift the virtual apex and the corresponding sector FOV from a first sector FOV that has at least one ultrasound obstructed region to a second sector FOV that encompasses the ultrasound obstructed region.

Abstract: An ultrasonic module includes a reception circuit adapted to receive a reception signal from an ultrasonic device, which receives an ultrasonic wave, to generate an echo signal, switching power supplies driven with a predetermined switching cycle, and adapted to supply the reception circuit with electrical power, and a phasing addition circuit adapted to perform an addition process on a first echo signal output when driving the reception circuit at a first drive timing in the switching cycle, and a second echo signal output when driving the reception circuit at a second drive timing delayed as much as a half cycle of a switching noise in the switching power supplies from the first drive timing.

Abstract: A base for an ultrasonic system comprises elements adapted to connect either a smart device or a display device to the base such that the base and smart device can be moved as a single unit. The base also comprises an ultrasonic array with at least one element capable of generating a signal in the range of 1 MHz to 15 MHz and a gimbal system configured to allow the ultrasonic array to be tilted relative to the base. The base provides a way for a physician to remotely control the transmitting angle and pressure exerted against the skin of an ultrasound transducer array of an ultrasound scanning system that is handheld by a patient.

Abstract: An ultrasound diagnosis apparatus which is connectable to a wireless probe that acquires first data by scanning an object is provided. The ultrasound diagnosis apparatus includes a controller which is configured to recognize an occurrence of a first event, to automatically terminate a first communication connection to the wireless probe via a first communication network, and to control an automatic start of a second communication connection to an external apparatus via the first communication network; and a communicator which is configured to exchange data with the wireless probe and/or with the external apparatus by using the first communication network under the control of the controller.

Abstract: The present invention comprises methods and devices comprising a scraping element used to contact circumferentially and longitudinally the surface walls of the uterine cavity to provide for broad contact of the intended surface with the device, resulting in attainment of a sufficient volume and comprehensive tissue sample for analysis as an endometrial biopsy or screening uterine cancer. The device may provide for a reservoir for the obtained sample to be contained when removing from the uterine cavity, cervical canal, and vagina. The device may be comprised of a detachable means or be of a material that allows the user to cut the sampling head of the device for placement in collection means to maximize the amount of tissue or cells being sent to the laboratory for analysis.

Abstract: A surgical device comprising: (1) a handpiece having a distal end portion; (2) a tubular member extending from the distal end portion, the tubular member having a lumen therethrough, the lumen comprising: (a) a proximal lumen portion, (b) a distal lumen portion, (c) a first central lumen portion, and (d) a second central lumen portion, the second central portion being located between the proximal lumen portion and the first central lumen portion, wherein the distal lumen portion diverges as the distal lumen portion extends away from the first central lumen portion in a distal direction, and the second central lumen portion diverges as the second central lumen portion extends away from the first central lumen portion in a proximal direction and; wherein the tubular member has wall with a substantially uniform thickness about the first central lumen portion.

Abstract: An electromechanical surgical system is disclosed including a hand-held surgical instrument, an end effector configured to perform at least one function, and a shaft assembly arranged for selectively interconnecting the end effector and the surgical instrument. The shaft assembly includes a linkage having a proximal housing and a distal housing at least partially received within the proximal housing. The distal housing is rotatable relative to the proximal housing and configured to selectively interconnect the end effector to the shaft assembly. The shaft assembly further includes a wire extending through the linkage having a central portion disposed within an annular groove defined between the proximal and distal housings. The central portion of the wire is annularly wound within the annular groove to define a coil. The coil is configured to at least one of radially expand and contract upon rotation of the distal housing relative to the proximal housing.

Abstract: The present disclosure relates to devices, systems, and methods for controlling the pressure a sensor applies on the surface of tissue to facilitate locating underlying pressure sensitive critical structures. The laparoscopic device includes a handle and a shaft extending distally from the handle. A flexible member is slidably disposed within the shaft and movable between a retracted position and an extended position. A sensor is coupled to a distal end of the flexible member. The flexible member is configured to flex to limit an amount of pressure applied by the sensor to a tissue surface when the sensor is in contact with a tissue surface.

Abstract: Disclosed is an implantable device (1) to be used in a human and/or animal body for occluding or partially occluding defective openings, hollow spaces, organ tracts, etc. or creating a defined connecting opening between walls, organs, hollow spaces, etc. Said implantable device (1) comprises a support structure which has a great length-to-width ratio along an axis (63) in a first operating state (primary shape) while having a smaller length-to-width ratio along said axis (63) in a second operating state (secondary shape). The support structure is provided with a proximal (20) and a distal section (30) and is formed from a single wire-type element (10) by intercoiling and/or intertwining and/or interweaving like a tissue and/or a cluster and/or a net. Also disclosed is a placing system especially for such an implantable device, comprising an advancing element (5), a directing wire (6,9) and/or an inner mandrin, and at least one holding wire (80,81).

Abstract: Tissue engagement devices can include a sheath, a first arm, a second arm and an actuation cannula. At least a proximal portion of each arm is within the sheath. The actuation cannula is also within the sheath, and can move within the sheath between a retracted position and an extended position. The actuation cannula moves at least a portion of each of the first and second arms into a region between an exterior surface of the actuation cannula and an interior surface of the sheath as the actuation cannula moves to the extended position.

Abstract: A surgical retractor system includes a substantially tubular retractor having several segments which can be irreversibly severed from one another to carry out a length adaptation of the retractor. A segment is subdivided into an expanding section and a plate section of differing radial flexibility and connected to each other in a one-piece material bond to allow plastic radial expansion of the retractor. An extractor can be operated to bring about plastic radial constriction of the retractor contrary to the radial expansion of the retractor. The extractor is prepared to cooperate with the plate section to bring about radial constriction of the retractor. A surgical instrument for removing a distractor or retractor from an opening includes at least one handle section defining a handle's longitudinal axis and at least one operating section defining a longitudinal effective axis, which are coupled to each other by a connecting section.

Abstract: A lateral retractor system for forming a pathway to a patient's intervertebral disc space includes a single dilator and a retractable dual-tapered-blade assembly. The dilator may feature a narrow rectangular body for insertion at an insertion orientation parallel to the fibers of the patient's psoas muscle, at an approximate 45-degree angle to the patient's spine. The retractable dual-tapered-blade assembly consists of only two blade subassemblies, each having a blade bordered by adjustable wings, along with built-in lighting and video capabilities. The dual-tapered-blade assembly may be passed over the single dilator at the insertion orientation and rotated approximately 45-50 degrees to a final rotated orientation parallel to the intervertebral disc space before the two blade subassemblies are retracted away from one another to create the surgical pathway, while simultaneously and continuously assessing for encroachment upon one or more nerve structures within 360-degrees of the instrument.

Abstract: The present teachings provide a flexible member securing assembly. The flexible member securing assembly includes a shaft, an arm extendable from the shaft, an anchor, and a flexible member grasper formed on a distal end of the arm. Methods of securing a flexible member are also provided.

Abstract: An apparatus includes a flexible fixation member having a body with a longitudinal extent and a width, the body defining a plurality of openings through the body, each of the plurality of openings formed substantially cross wise through the width of the body, and a suture having two terminal ends, the suture being interwoven through each of the plurality of openings in the body of the fixation member such that multiple portions of the fixation member are slidably coupled to the suture and configurable to form a cluster within a surgical site.

Abstract: Surgical devices and methods of soft tissue repair using pre-looped tensionable and non-pre-looped tensionable knotless fixation devices. A flexible material (for example, suture or suture tape) may be attached to the fixation device. A flexible material may be threaded through an eyelet of a tip provided as part of a swivel anchor assembly to provide added stability to the fixation devices.

Abstract: The present invention provides suture retention devices for retaining a suture on a bodily wall, e.g. for affixing the suture to the skin such as during the creation of an external percutaneous fluidic connection. In one embodiment, a device includes a base member and a swivel member. In another embodiment, the device includes a base member, first and second jaws, and a key. Operation of the swivel member or key serves to lock the suture to the device, and hence maintain tension on the suture while affixed to the skin.

Abstract: A suture anchor includes a tubular anchor body made of suture material, the tubular anchor body having a partially open distal tip and a bore extending through the tubular anchor body to a proximal end of the tubular anchor body and a suture woven from the distal tip and extending through the bore and exiting through the proximal end, the suture forming a suture loop outside of the distal tip. The tubular anchor body is configured such pulling an end of the suture at the proximal end causes the tubular anchor body to collapse.

Abstract: Surgical constructs and methods are provided for securing soft tissue to bone. One exemplary embodiment of a construct is formed from a suture filament and includes two terminal ends of filament and an intermediate portion disposed along at least a portion of a length extending between the terminal ends. The construct can have a first terminal end that is the first terminal end of the filament, and a second terminal end that includes a loop. The loop can be formed by disposing the second terminal end of the filament within a volume of a portion of the intermediate portion of the filament. In some disclosed methods, both terminal ends of the filament can be passed through tissue when performing soft tissue repairs. Various other embodiments of constructs and methods are provided, including constructs having two or more filaments associated with an anchor and methods of using such constructs.

Abstract: An anchoring system is a combination of a nanofiber scaffold material and an arthroscopically deployable suture anchor. The anchor is deployed into a bone tunnel using common techniques. The nanofiber material extends out of the proximal end of the implant, once deployed. The implant also includes pre-loaded sutures or has the ability to accept and lock sutures to the implant. For an implant pre-loaded with suture, the implant is placed into the bone, the material is deployed above the anchor onto the surface of the bone, suture is passed through the soft tissue, and knots are tied to secure the tissue against the bone, sandwiching the material between the bone and tissue, to provide a pathway for cells from the bone marrow to the soft tissue-bone interface, promote the healing response, provide a biomimetic structure that cells readily adhere to, and create a larger healing footprint.

Abstract: Driver assemblies are configured to protect a threaded sleeve of an anchor from damage due to over-insertion. An internal spring permits axial retraction of an outer shaft coupled to the sleeve independent of the inner shaft and the handle. Connection members extending along the spring create an axial stop between a drive housing and a center housing of the driver assembly. The drive housing is allowed to travel proximally in response to axial loading against the spring, while travel distally is limited by the engagement between the connection members and receivers on the center housing.

Abstract: The present disclosure concerns a suture anchor including a distal body and a proximal body. The distal body defines a bounded transverse eyelet therethrough and the proximal body defines an unbounded transverse eyelet therethrough at a distal end thereof the unbounded transverse eyelet being unbounded distally. The proximal body is cannulated for receiving a proximal portion of the distal body through the cannula, whereby the eyelets are configured for alignment with one another to as to enable receiving a suture therethrough. Once the suture is received, the distal body and proximal body may be rotated relative to one another along a longitudinal axis of the suture anchor such that the eyelets are rotated out of phase with one another causing the suture to wrap around the proximal portion of the distal body and pinching the suture between an outer surface of the distal body and an inner surface of the proximal body. This has the advantage of causing the distal end of the proximal body to expand.

Abstract: A medical suturing instrument in which the movement of an operation part is transmitted with a time lag to a loop forming part and a suture thread by means of a loop feed/return mechanism and a suture thread feed mechanism, and once a loop has been fed out from the tip end of a loop introduction needle, the suture thread is fed out from the tip end of a suture thread introduction needle.

Abstract: A distal tip for a suture securing tube is disclosed. The distal tip has a flared distal end and a distal opening in the flared distal end. The distal tip also has a tube interface opening in a proximal end. The distal tip further has a channel coupling the distal opening to the tube interface opening. The distal tip also has one or more crimp windows.

Abstract: Suture locking clamps for securing prostheses such as heart valves or annuloplasty rings with sutures and without using knots improve the ease of implantation. The clamps have opposed clamp halves separated by a slot opening to one side and surrounded by a biasing member such as one or more C-clip springs. Sutures pass laterally into the slot which is held open by a retention member positioned between the clamp halves. The locking clamp slides along the sutures into position, the tension of the sutures is adjusted, and the retention member removed to allow the biasing member to clamp the sutures between the clamp halves. A delivery tool used to deliver and deploy the locking clamps contains a number of clamps within a delivery tube in a stack and bonded together for safety and a common retention member. The tool has a longitudinal channel on one side for entry of sutures.

Abstract: A suturing device includes a housing, a rod, a ferrule assembly, and a needle. The housing defines a guide lumen extending longitudinally therethrough. The rod is engaged with the housing and extends distally therefrom. The ferrule assembly is disposed at a distal end of the rod and is configured to releasably retain a ferrule therein. The ferrule is adapted to retain of a portion of a suture therein. The needle is configured for translation through the guide lumen defined within the housing. A distal end of the needle is configured to engage the ferrule within the ferrule assembly for removal of the ferrule from the ferrule assembly.

Abstract: A method of implanting a penile prosthesis includes providing a tool including a needle having a locking groove formed in a shaft of the needle, where the locking groove has a ridge or a notch. The method includes accessing a penile implant having a length of suture coupled to a distal end of the penile implant, securing the length of suture into the locking groove of the needle; inserting the tool and the needle into a corpora cavernosum of a penis; passing the needle and the length of suture through a glans of the penis; disengaging the length of suture from the locking groove of the needle; and pulling the penile implant into the corpora cavernosum of the penis with the length of suture.

Abstract: A loading unit for engagement with a surgical instrument, and including single and double retention slots. At least one single retention cavity includes a first retention guiding surface configured to engage a first pusher guiding surface of a single pusher retained therein, a second retention guiding surface configured to engage a second pusher guiding surface of a single pusher retained therein, a third retention guiding surface configured to engage a third pusher guiding surface of a single pusher retained therein, and a fourth retention guiding surface configured to engage a fourth pusher guiding surface a the single pusher retained therein. At least one double retention cavity includes a first retention guiding surface configured to engage a first pusher guiding surface of a double pusher retained therein, and a second retention guiding surface configured to engage a second pusher guiding surface of a double pusher retained therein.

Abstract: A surgical tool is provided comprising: a jaw assembly that includes a first and second elongated jaws each having a proximal end and a distal end, wherein the proximal end of the first jaw is mounted to be rotatable about a pivot axis between an open position and a closed position; first parallel side edges secured to the first jaw that extend parallel to a longitudinal first axis of the first jaw; second parallel side edges secured to the second jaw that extend parallel to a longitudinal second axis of second jaw; a slider beam that includes a cross-beam portion sized to slidably fit between the first parallel side edges and between the second parallel side edges, a first transverse beam configured to slidably engage surfaces of the first parallel side edges facing away from the second jaw, and a second transverse beam configured to slidably engage surfaces of the second parallel side edges facing away from the first jaw; a pulley rotatably mounted to the distal end of the first jaw; and a first slider cabl

Abstract: A surgical tool assembly is disclosed. The surgical tool assembly can include an end effector comprising an elongate channel configured to receive a fastener cartridge, and the elongate channel can comprise a brace. The surgical tool assembly can also include a shaft comprising an articulation drive assembly, wherein the articulation drive assembly comprises an articulation link pivotably coupled to the elongate channel. The articulation link comprises a pocket configured to receive the brace when the end effector is in a fully articulated configuration. The brace and the pocket can define complementary planar surfaces for resisting rotation of the brace within the pocket to resist de-articulation of the end effector when it is in its fully articulated configuration.

Abstract: A surgical instrument includes a body, a shaft assembly, an end effector, and an electrical contact assembly. The includes a power source, while the shaft assembly extends distally from the body. The end effector includes a channel assembly and a cartridge assembly configured to selectively couple with the channel assembly. The cartridge assembly includes an electrically activated component. The electrical contact assembly is capable of electrically coupling the power source with the electrically activated component of the cartridge assembly. The electrical contact assembly includes a first electrical contact, a second electrical contact, and an insulating membrane. The first electrical contact is associated with the channel assembly while the second electrical contact is associated with the cartridge assembly. The insulating membrane is associated with either the first electrical contact or the second electrical contact.

Abstract: A surgical instrument includes a body assembly, a shaft assembly extending distally from the body assembly along a shaft axis, and an end effector at a distal end of the shaft assembly. The shaft assembly includes an outer tube configured to rotate relative to the body assembly about the shaft axis. The surgical instrument further includes a slip ring assembly configured to enable electrical communication between the shaft assembly and the body assembly while permitting relative rotation therebetween. The slip ring assembly includes a first electrical contact supported by the outer tube, and a second electrical contact electrically coupled with the first electrical contact and positioned radially outward of the outer tube. The first electrical contact is configured to rotate with the outer tube about the shaft axis relative to the second electrical contact while the first and second electrical contacts remain electrically coupled.

Abstract: Devices, tools, systems, kits and methods for closing a tissue opening non-invasively are presented. The devices include a tissue closure device that reliably induces eversion of tissue edges that define a tissue opening.

Abstract: A device (10) for repair of a heart valve leaflet includes an elongated body (12) having a lumen (16) extending therethrough in a longitudinal direction, a proximal end, an open distal end (19). A core (11) is disposed within the lumen, and is operable to spin about an axis extending in the longitudinal direction. The spinning of the core draws a portion of the heart valve leaflet into the lumen through the open distal end of the body and secures the portion of the heart valve leaflet to the core in a gathered configuration.

Abstract: An anastomosis prosthesis comprising a tubular member with a leading end comprising a leading edge, and a trailing end comprising a trailing edge, wherein the leading end of the tubular member is reversibly, radially compressible, and the leading edge of the tubular member is provided with one or more radially outwardly directed flexible, substantially linear anchoring members. The anchoring members are initially arranged at an angle in relation to a longitudinal axis of the tubular member such that the anchoring members point in the direction of the trailing end of the tubular member.

Abstract: An exemplary tissue compression device for forming an anastomosis includes a first device portion having a first mating surface, a first base wall recessed from the first mating surface so as to define a first inner recess, and a first set of suture bores extending through the first base wall and opening to an outer periphery of the first device portion. A second device portion of the device has a second mating surface, a second base wall recessed from the second mating surface so as to define a second inner recess, and a second set of suture bores extending through the second base wall and opening to an outer periphery of the second device portion. The first and second device portions are configured to compress tissue positioned between the first and second mating surfaces.

Abstract: An apparatus includes a handle assembly, an end effector, a firing assembly, and a release assembly. The handle assembly includes first and second arms and a latching lever. The end effector includes first and second jaws. The firing assembly is configured to sever tissue captured between the jaws. The release assemble is configured to urge the latching lever away from the first arm to pivot the second jaw from a fully closed position to a partially closed position.

Abstract: A surgical instrument includes an anvil selectively coupleable to a stapling head assembly and a trigger operable to fire staples into tissue compressed between the anvil and the stapling head assembly. In some versions, a lockout member may engage a securing feature to prevent actuation of the anvil relative to the stapling head assembly. For instance, a tab may engage a slot on an actuator, a screen door lock may provide frictional resistance or engage teeth on the actuator, a door may actuate into engagement with one or more recesses, geared teeth may mesh with teeth on the actuator, the lockout member may include a ratcheting assembly to engage actuator, and/or a push button may actuate into a recess while disengaging the lockout member. Alternatively, in some versions, the trigger actuation assembly may be disengaged prior to firing. An anvil position indicator may restrict engagement of the trigger actuation assembly.

Abstract: An epicardial implant having a positioning device that defines an open interior. The positioning device is configured to be detachably coupled with an implant delivery device such that the positioning device may be detached from the implant delivery device after the implant is in place about an atrial appendage. The positioning device has first and second sides with a distal end that couples the first and second sides. The implant includes an expandable cuff coupled with the positioning device. The positioning device is configured to selectively move the expandable cuff toward and away from an atrial appendage to position the expandable cuff in a desired position relative to the atrial appendage. The expandable cuff is expandable into at least a portion of the open interior of the positioning device to physically occlude a base of the atrial appendage following placement of the expandable cuff into the desired position.

Abstract: This disclosure concerns release mechanisms for medical implants, particularly embolic coils and the like, which utilize bulbous elements and receiving elements to constrain the bulbous elements. In some cases, the receiving elements are sized and shaped to help constrain the bulbous element axially and/or radially, and may work in concert with constraining elements and/or release wires that are optionally moveable independently of the receiving elements.

Abstract: Apparatus for percutaneously occluding a hollow structure, said apparatus comprising: an occluder, said occluder comprising a first component and a second component, wherein said first component is configured so that it may assume (i) a diametrically-reduced configuration for disposition within the lumen of a hollow tube, and (ii) a diametrically-expanded configuration for disposition adjacent to the hollow structure, whereby to occlude the hollow structure, and further wherein said second component percutaneously connects said first component to a site remote from said first component.

Abstract: System for fixation of leaflets of a heart valve including a delivery catheter having an elongated shaft, a proximal end portion and a distal end portion configured to be positioned proximate native leaflets of a heart valve from a remote vascular access point, and a fixation device releasably coupled to the delivery catheter. The fixation device includes a first arm moveable between a closed position and an open position, and a second arm moveable between a closed position and an open position. The fixation device further includes a first gripping element movable relative to the first arm in the open position, the first gripping element biased toward the first arm to capture a first leaflet of the heart valve therebetween, and a second gripping element movable relative to the second arm in the open position, the second gripping element biased toward the second arm to capture a second leaflet of the heart valve therebetween.

Abstract: A device for treating a tissue opening includes a proximal portion including an elongated flexible member, a capsule releasably coupled to a distal end of the flexible member and including a lumen extending therethrough and a clip including a pair of arms movably housed within the capsule. A suture extending along a first one of the pair of arms and including a loop at a distal end thereof extending across an opening extending through the first one of the pair of arms. A suture grabbing element extending laterally from a second one of the pair of arms and including a hook so that, when the pair of arms are moved toward a closed configuration, the hook extends through the opening to grab the loop and draw the distal end of the suture from the first one of the pair of arms toward the second one of the pair of arms.

Abstract: A device for transcatheter gathering of tissue of a heart valve leaflet may include an elongated tube extending in a longitudinal direction and having an open distal end, a tissue securing component disposed at the distal end of the elongated tube, and a capture tool movable in the elongated tube between a retracted position and an extended position. The elongated tube may have an inner surface and a lumen extending therethrough. The tissue securing component may include a clip having a roller and a support element. The roller may be rotatable relative to the support element. The capture tool may be operable to capture tissue of the heart valve leaflet and to draw the captured tissue into the tissue securing component. The tissue securing component may be adapted to be applied to the captured tissue to hold the captured tissue in a gathered configuration.

Abstract: A medical instrument comprising: (a) a first joint comprising a first member and a second member, the first member configured to be repositionable with respect to the second member in a first degree of freedom; (b) a second joint operatively coupled to the first joint, the second joint comprising a third member and a fourth member, the third member configured to be repositionable with respect to the fourth member in a second degree of freedom; (c) a pair of repositionable jaws operatively coupled to the first joint and the second joint; (d) an occlusion clip detachably mounted to the pair of repositionable jaws; and, (e) a controller operatively coupled to the first joint, the second joint, and the pair of repositionable jaws, the controller including a first control configured to direct repositioning of at least one of the first member and the second member, and a second control configured to direct repositioning of at least one of the third member and the fourth member, and a third control configured to dir

Abstract: The invention relates to a haemostatic bracelet (1) comprising: —a clamp comprising two branches (11, 12) and a first strut (13), each branch (11, 12) being connected by one of its ends to the other branch by means of the first strut (13), —a compression element (24) placed, when the bracelet is ready for use, inside the space defined by the branches (11, 12) and the first strut (13) of the clamp or inside a projection of this space, the compression element (24) protruding in the direction of the opening between the ends of the branches (11, 12) of the clamp opposite to the first strut (13), —actuation elements (30, 40) fixed to the branches (11, 12) of the clamp so that the ends of the branches (11, 12) of the clamp opposite to the first strut (13) can be spread by moving the ends of the actuation elements towards each other.

Abstract: The invention relates to a medical device with a machine element mounted so as to be linearly movable and at least one linear guide, comprising at least one ball bearing and defining a longitudinal axis, for guiding a linear movement of the machine element parallel to the longitudinal axis, said at least one ball bearing comprising a plurality of balls which are movably held in corresponding ball holders and which guide the machine element, wherein the plurality of ball holders are constructed in the form of elongated holes.

Abstract: Disclosed is a method of simulating mastication. The method includes obtaining computer-readable three-dimensional representations of a first skeletal fragment including a portion of at least one of a mandible and a maxilla and of a recipient skeletal fragment including a portion of at least one of a mandible and a maxilla. The method also includes obtaining placement data and obtaining muscle insertion data. The method also includes simulating a contraction of a muscle positioned according to the muscle insertion data in a representation of a surgical hybrid comprising at least a portion of the first skeletal fragment positioned according to the placement data relative to at least a portion of the recipient skeletal fragment. The method also includes outputting a representation of mastication represented by the simulating.

Abstract: An orthopaedic surgical instrument comprising a metallic customized patient-specific surgical instrument is disclosed. The metallic customized patient-specific surgical instrument includes a base plate sized to be positioned on a resected surface of a distal end of a patient's femur, an anterior resection guide body attached to, and extending from, the distal surface of the base plate to a free distal end, a posterior resection guide body attached to, and extending from, the distal surface to a free distal end, and a pair of chamfer resection guide bodies attached to, and extending from, the distal surface.

Abstract: A method of producing a coil for a flexible drive shaft includes: winding a roving into at least one helical groove of a mandrel; coating the roving with an uncured material; heating the coated roving to a curing temperature in the at least one helical groove of the mandrel to cure the uncured material and form a composite roving; and stripping the composite roving from the mandrel. A method of forming a flexible driveshaft for a surgical instrument is also provided and includes: feeding a plurality of flexible coils into a feeder such that each of the plurality of flexible coils are spaced from one another about a rod; rotating the rod to wind the plurality of flexible coils about the rod; and binding the wound plurality of flexible coils and rod together.

Abstract: A glenoid reamer having a rim, a hub located central to the rim, a plurality of cutting blades, each of the blades extending from the rim to the hub, and a first transverse slot and a second transverse slot, wherein the first and second transverse slots are positioned to bisect the rim. The glenoid reamer can be configured to slide over a guide pin and toggle with respect to the guide pin, such that the guide pin is received in the first and second transverse slots and the reamer is substantially parallel with the guide pin. The glenoid reamer can also be configured to toggle with respect to the guide pin, such that the reamer is substantially perpendicular with respect to the guide pin.