Abstract: A fluid displacement and pressurizing device which includes a housing, a first piston in the housing, a plunger which extends from the housing and has a second piston thereon, and an actuator that works to selectively lock the piston to either the housing or the plunger depending on the position of the second piston in the housing. Effectively, the actuator includes a first locking mechanism that locks and unlocks the first piston relative to the housing and a second locking mechanism that locks and unlocks the plunger relative to the piston. As such, the first locking mechanism is not only a locking mechanism but is also an actuating mechanism with regard to actuating the second locking mechanism.

Abstract: Devices including a capsule having an interior and a clamp assembly including a plurality of clamps. Each clamp includes a first arm having a first free end and a second arm having a second free end. The device includes a clamp assembly including a compacted state in which the plurality of clamps are compressed within the capsule and a deployed state in which at least the free ends of the plurality of clamps are positioned outside of the interior of the capsule. The first free end is closer to the second free end in the compacted state as compared to the deployed state. The device can further include a push rod releasably secured to the clamp assembly and a delivery rod releasably secured to the capsule. Methods of using the devices are also disclosed.

Abstract: Proposed is a biliary stent unit having a pulling string that is fixed to the skin of a human body to prevent a stent from separating from a diseased part of the biliary tract, and having a soft tube that reduces stimulus in the human body after a surgery because it has flexibility.

Abstract: The present disclosure provides a glenoid implant system for a reverse shoulder implant system that includes a glenoid implant having a center post, and also includes an angled baseplate comprising a bone facing surface to face an implant site prepared in a glenoid region of a patient, and an implant facing surface to face and engage the glenoid implant and receive the center post of the glenoid implant, wherein the implant facing surface being at an angle with respect to a centerline of the bone facing surface.

Abstract: A fluid displacement and pressurizing device which includes a housing, a first piston in the housing, a plunger which extends from the housing and has a second piston thereon, and an actuator that works to selectively lock the piston to either the housing or the plunger depending on the position of the second piston in the housing. Effectively, the actuator includes a first locking mechanism that locks and unlocks the first piston relative to the housing and a second locking mechanism that locks and unlocks the plunger relative to the piston. As such, the first locking mechanism is not only a locking mechanism but is also an actuating mechanism with regard to actuating the second locking mechanism.

Abstract: The present invention relates to a shoulder prosthesis comprising:—a metaglene element (2) or baseplate;—a pin (3) projecting from said metaglene element (2);—a through-hole (11) in the centre of said metaglene element (2);—at least one through-hole (5) formed in a periphery of the metaglene element (2) with respect to said central through-hole (11);—a glenosphere element (12) opposite said pin (3) with respect to said metaglene element (2);—a central compression screw (9) housed in said through-hole (11) in the centre of said metaglene element (2) and having a head abutting onto the bottom of said hole (11); and—wherein the central through-hole (11) has an opening (11A) that is threaded in a stretch to receive the end of a safety screw (18) passing through the glenosphere element (12);—a connector element (13) between the metaglene element (2) and the glenosphere element (12), the metaglene element (2) providing a seat (14) for housing the connector element (13) projecting around the central through-hole (11

Abstract: Implant assemblies for reverse shoulder arthroplasty are disclosed. In one embodiment, the implant assembly comprises a humeral component, an adaptor fixed to the neck of the humeral component, and a glenosphere bearing component coupled to the adaptor. The glenosphere bearing component comprises a first bearing surface that interfaces with an articulating surface of the adaptor to allow the adaptor to rotate relative to the adaptor and humeral component. The adaptor and the glenosphere bearing component form a locking mechanism that prevents the adaptor from decoupling from the glenosphere bearing component while allowing the adaptor to remain rotatable relative to the glenosphere bearing component after the implant assembly is implanted in the patient The second bearing surface is configured to interface with a glenosphere component to allow the glenosphere bearing component to articulate relative to the glenosphere component.

Abstract: A modular system for total knee arthroplasty includes a modular trial implant assembly. The modular implant assembly includes an elongate shaft configured for insertion into an elongate cavity in a bone, a reamer removably coupleable to the elongate shaft via a connection that allows the reamer to rotate while the elongate shaft remains in a substantially fixed angular orientation. The reamer has an outer surface that tapers toward the distal end configured to form a tapered cavity in an end of a bone in which the reamer is inserted and rotated. The modular trial implant assembly further includes a trial implant removably coupleable to a proximal end of the reamer. A modular final implant assembly includes an elongate stem, a tapered body and an implant body, each having a size and shape that can substantially correspond to a size and shape of the elongate shaft, the reamer and the trial implant, respectively.

Abstract: A total knee implant prosthesis is disclosed. The total knee implant prosthesis includes a tibial component including a pair of bearing surfaces and a post positioned between the bearing surfaces, and a femoral component configured to rotate relative to the tibial component. The femoral component includes a pair of condyles sized and shaped to articulate on the bearing surfaces and a cam positioned between the pair of condyles. The cam engages the post at a first contact point when the femoral component is at 0 degrees of flexion and engages the post at a second contact point located lateral of the first contact point when the femoral component is at a first degree of flexion greater than 0 degrees. The cam is disengaged from the post when the femoral component is at a second degree of flexion greater than the first degree of flexion.

Abstract: Embodiments of the invention described herein thus provide implants and methods for manufacturing an implant having an outer layer that is porous. The porous outer layer can help encourage tissue ingrowth into the implant. The porous outer layer may be positioned around a core structure this is solid or that has a hollow interior. The core structure may be spherical or any other appropriate shape for a medical implant.

Abstract: Compositions and methods thereof include bone fibers made from cortical bone in which a plurality of bone fibers are made into shapes that are used to augment fixation of orthopedic implants and screws. Sheets of bone fibers may be used as an interface between bone and tissue, tendons, and/or ligaments. Cylindrical shaped implants that may be placed in drilled holes in bone prior to screw placement to enhance fixation of the screw. The physical presence of the fibers provides initial fixation, while the use of an osteoinductive material provides long term enhancement of bone formation around the screw and hence fixation. The bone fiber compositions may be in the form of a cylinder or a tube. A delivery system and methods of use are also provided.

Abstract: Disclosed is a motorized assistance system with a tibial orthosis including: a tibial fastening that covers the user's shin; an ankle fastening articulated with a plantar fastening at the axis of the ankle; and a processor. The tibial fastening can include a support of a motorized winch, in which a strap is hooked, whose free end is fixed to the foot, so that the winch takes up the strap when a foot position sensor indicates that it is not resting on the ground. Alternatively, the system can have a femur orthosis with two femur actuators that take up or release two strap in parallel, one attached to a harness or belt and the other to the tibial fastening. The system may include additionally or alternatively a hip orthosis.

Abstract: A vascular prosthesis includes an outer crimped textile graft and an inner polymeric liner. The polymeric liner is secured to the valleys of the crimps of the textile graft while leaving the peaks of the textile graft free of the liner. The polymeric liner is impermeable to blood flow. The inner liner may include expanded polytetrafluoroethylene polymer, and the graft may include polyethylene terephthalate yarns.

Abstract: Devices, systems and/or methods for fixating soft tissue to bone are provided. In one embodiment, a repair device for fixating soft tissue to bone with a bone anchor includes a soft tissue anchor and one or more flexible members. The soft tissue anchor includes a base with multiple legs extending from the base. The one or more flexible members are coupled to the base and configured to extend from the base to the bone anchor with a fixed length. With this arrangement, the fixed length of the one or more flexible members is configured to maintain a substantially fixed pre-determined distance between the soft tissue anchor and the bone anchor such that, as the bone anchor is seated into bone, the one or more flexible members pulls the soft tissue anchor down against the soft tissue to fixate the soft tissue to the bone.

Abstract: Stents are disclosed herein. The stents described herein can comprise a hollow cylindrical body in which a middle region extends to a first end and also extends to an opposing second end. The first end and the second end can each comprise a plurality of flanges, within which the flanges can have either similar or different characteristics, particularly physical profiles.

Abstract: The present invention provides an anchor delivery device for repairing a heart valve, and relates to the technical field of medical instruments. The system comprises a bend adjustable tube assembly, an anchor delivery assembly, a suture locking mechanism, and a puncture assembly. The anchor delivery assembly is mounted in the bend adjustable tube assembly; the suture locking mechanism is connected to an anchor, and is provided with a guide portion located in the anchor; and the puncture assembly is mounted in an anchor delivery tube, and a puncture needle body of the puncture assembly penetrates the guide portion and is radially limited by the guide portion. According to the present invention, the puncture accuracy of the puncture needle body and the stability thereof after puncture can be ensured, and the accuracy and stability of the subsequent implantation of the anchor are improved.

Abstract: A clamping instrument (10), mainly comprising: a clamping base (20), a driving base (30), a clamping structure (40), which forms different clamping angles according to the distance between the clamping base (20) and the driving base (30); and a fine adjustment member (50), wherein the fine adjustment member (50) and the driving base (30) can be separated from each other or connected to each other, such that the driving base (30) can move rapidly or step by step relative to the clamping base (20), thereby achieving the aim of rapidly adjusting or finely adjusting the clamping angle of the clamping structure.

Abstract: An acetabular shell insertion tool with an anti-rotation feature is provided. The insertion tool attaches to an acetabular shell including a center hole having an internal threading and an anti-rotation recess disposed around the center hole and having a predetermined shape. The insertion tool includes an outer shaft and an inner shaft disposed within the outer shaft. The outer shaft has an anti-rotation projection shaped to be received in the anti-rotation recess of the acetabular shell so as to prevent rotation of the outer shaft relative to the acetabular shell, thereby preventing the insertion tool from disengaging from the shell. The inner shaft has a threaded tip adapted to be threaded into the internal threading of the center hole to lock the insertion tool to the acetabular shell.

Abstract: A fixing device for clamping a tissue comprises a support mechanism comprising a fixed connecting assembly and a drive assembly, and a clamp mechanism comprising closure members and capture portions, wherein each closure member comprises a closure connecting portion and a closure clamping portion in cooperation with one of the capture portions to clamp the tissue; wherein each closure connecting portion is provided with guide slots comprising a first slot portion and a second slot portion in communication therewith and has a relatively smaller radian, the fixed connecting assembly is provided with pins at least partially located in the guide slots, respectively, and the pins are slidable relative to the guide slots when the drive assembly moves relative to the fixed connecting assembly, so as to drive the closure clamping portions to move towards or away from each other. A system comprising the fixing device, and a method are provided.

Abstract: Embodiments of a Urological implant include an implant with an elongated body having a longitudinal axis. Optionally longitudinal ribs symmetrically oppose each other and are connected to elongated body. The longitudinal ribs are optionally elastically shiftable between a collapsed state and an expanded state relative to the spinal longitudinal axis, in order to retract or/and support periurethral tissue. Optionally the system includes an implant extraction handle. The extraction handle is optionally positioned proximally to the elongated body and connected to the longitudinal rib and subject to a pulling force to facilitate and/or force approximation of the longitudinal supports to the longitudinal axis. In some embodiments, an implant body includes longitudinally spaced arched members, interconnected via arch ends sequentially along a length of a first and second longitudinal rib.