Abstract: A total knee replacement system including a distal femoral knee replacement component and a tibial component having a bearing surface and a tibial post with a posterior surface, wherein the distal femoral knee replacement component includes a body having a pair of medial and lateral condylar protrusions and an intercondylar region therebetween dimensional to receive the tibial post, the body further having a cam mechanism bridging the intercondylar region, the cam mechanism having a least a first, second and third cam surface areas, with each having a convex shape in the sagittal plane with different centers of radius wherein none of cam surface areas engage the posterior surface of the tibial post when the knee is in extension and wherein the cam mechanism includes at least one concave cam surface area between at least two of the three convex cam surface areas.

Abstract: Systems and methods for preparing a ligament graft construct for a ligament reconstruction or repair procedure are provided. In general, the described techniques utilize a reinforcement material having at least one suture tail extending therefrom. The reinforcement material is a ribbon or a ribbon-like flattened portion attached to or integrally formed with the at least one suture tail. To prepare a tissue repair construct, the reinforcement material is positioned on a first surface of a graft to extend from an end thereof and the at least one suture tail, coupled to a needle, is repeatedly passed through the reinforcement material and the surface of the graft to a second surface of the graft, and around a side portion of the graft to thereby create multiple suture loops. The tissue repair construct can be formed on each end of the graft.

Abstract: A mechanical prosthetic heart valve, includes an annular support on which at least two movable flaps and several articular extensions are arranged in an articulated manner. Each flap includes a central part framed by two lateral wings that each cooperate with an articular extension by way of an end portion that has an articulation facet. The two articulation facets of each flap together make up a surface area of less than 5% of the total outer surface area of the flap.

Abstract: Embodiments of the invention include a system and method for coupling a graft to a bone. A graft preparation tool may be used to place one or more holes in a graft and an offset measurement tool may be used to determine the distance of the one or more holes from an edge of the graft to be aligned with a portion of the bone. One or more complementary holes may then be created in the bone and fasteners applied through the holes to couple the graft to the bone.

Abstract: The present disclosure relates to a surgical device, such as a surgical implant, which may be used in several types of procedures. More specifically, the present disclosure relates to implants for use in an anterior, posterior, posterior lateral or direct lateral approach to the disc space. The surgical device may be manipulated in various manners to accommodate delivery through a minimally invasive portal in one configuration and adjusted to a second configuration once placed in the intervertebral space. A delivery system for placing the surgical device in a body is also disclosed.

Abstract: A method of implanting a prosthetic knee joint assembly. The method includes: coupling a femoral component to a femur, and coupling a tibial component to a tibia; coupling a ligament link to one of the femur or the tibia; coupling the ligament link to a coupling component of one of the femoral component or the tibial component; arranging the ligament link in a first position relative to the tibial component when the prosthetic knee joint assembly is implanted in a left knee; and arranging the ligament link in a second position relative to the tibial component when the prosthetic knee joint assembly is implanted in a right knee, the second position is different from the first position.

Abstract: A system and method for making an orthopedic repair by fixing a soft tissue graft to bone, utilizes an implant including a body wedge having first and second outwardly expandable wedge portions, a wing portion having outwardly expandable wings, and a deployment member which is movable distally into the implant to deploy the wedge portions and the wings into an expanded deployed orientation.

Abstract: Disclosed is a valve (502) for short time replacement, for taking over the function of and/or for temporary support of a native valve in a heart, the valve being positioned through the native valve upon implantation, the valve comprising an at least partially collapsible and/or at least partially expandable tube (602) and a flange (708). The valve allows for fast and easy replacement of a native valve, and more time for medical personnel to make decisions, prepare and/or perform surgery/medical intervention. Thus, the valve may provide for an improved quality of surgery/medical intervention.

Abstract: An implantable endoluminal prosthesis for replacing a damaged aortic valve is provided. In one embodiment, the prosthesis includes a balloon-expandable stent, a tubular conduit that extends into the ascending aorta, and a self-expanding stent. The tubular conduit extends across the balloon-expandable stent. The tubular conduit includes an artificial valve. The self-expanding stent extends across the tubular conduit into the ascending aorta. The balloon-expandable stent, the tubular conduit, and the self-expanding stent are coupled to provide unidirectional flow of fluid into the aorta and further into the coronary arteries. Also provided is a method for implanting the endoluminal prosthesis.

Abstract: An orthotopic artificial bladder endoprosthesis includes a casing defining an enclosure for containing the urine of a patient; the casing being made of a PGA fiber fabric; two first connectors connected to the casing and connectable to the ureters of the patient to allow the entrance of the urine into the enclosure; a second connector connected to the casing and connectable to the patient's urethra to allow the outflow of the urine from the enclosure; a catheter inserted in the enclosure through the second connector and including a duct and an expandable element in fluid communication with the duct.

Abstract: A prosthetic mitral valve with a compressible and expandable stent that, when expanded, is circumferentially oval, elliptical, or D-shaped, with a major axis and a minor axis ratio of from about 3:4 to about 4:5. Embodiments of the stent comprise three commissure regions disposed towards an outflow end and three curved cusp regions between adjacent commissure regions. Three flexible leaflets are attached to the commissure regions in a tri-foil configuration. Embodiments of the prosthetic mitral valve include an atrial ring disposed at the inflow end of the stent.

Abstract: A plurality of individual tools is provided where each tool is uniquely configured to perform a step or a portion of a step in a novel procedure associated with the implantation of a stabilizing device (e.g., an interspinous spacer) for stabilizing at least one spinal motion segment. The tools are usable individually, or more preferably as a tooling system in which the tools are collectively employed to implant an interspinous spacer, generally in a minimally invasive manner. For example, each of the tools is arranged with coordinated markings and/or other features to ensure consistent depths of insertion, proper orientation of the tools with respect to each other or an anatomical feature of the patient, and precise delivery of the spacer to maintain safe positioning throughout the implantation procedure.

Abstract: A polyaxial bone screw assembly includes a receiver, a shank, an articulation structure for retaining the shank in the receiver and a compression insert for engagement with a longitudinal connecting member such as a rod. The articulation structure includes substantially spherical convex and concave surfaces that slidably engage both shank and receiver surfaces to provide compound articulation between the receiver and the shank. The receiver includes inwardly directed spring tabs engaging the insert and prohibiting rotation of the insert within the receiver.

Abstract: A Variable Angle Surgical Instrument is disclosed and generally comprises: a rail portion including a proximal end, a distal end, and a longitudinal axis extending therebetween; a jaw portion operably coupled to the distal end of the rail portion; wherein the jaw portion rotates to variable angles relative to the longitudinal axis, and the jaw portion operates between a closed position and an open position to clamp down and remove tissue; a locking mechanism operably coupled to the rail portion to lock the jaw portion to an angled position.

Abstract: The present invention provides an artificial joint, including a femur connecting device, a tibia connecting device, and a receiving device, wherein the femur connecting device is connected and fixed with the receiving device and the tibia connecting device via a fixing member unparallel to a joint-twisting axis, and wherein cushion member receives the femur connecting device via a pivot-receiving surface and receives the tibia connecting device via a twist-receiving surface, thereby providing an durable and reliable artificial joint.

Abstract: A lung volume reduction system is disclosed having an implantable device adapted to be delivered to a lung airway of a patient in a delivery configuration and to change to a deployed configuration to bend the lung airway. The invention also discloses a method of bending a lung airway of a patient by inserting a device into the airway in a delivery configuration and bending the device into a deployed configuration, thereby bending the airway.

Abstract: Prosthetic devices and frames for implantation at a cardiac valve annulus are provided that include an annular frame (having an inflow end and an outflow end) and a plurality of axial frame members that bridge two circumferentially extending rows of angled struts. The axial frame members can include a plurality of axially extending leaflet attachment members and a plurality of axial struts in a 1:1 ratio. Along each of the two rows, the frame can have at least three angled struts between adjacent axial frame members.

Abstract: An orthotopic artificial bladder endoprosthesis includes a base obtained with a multi-layered silicone membrane having an external surface and an internal surface both coated with pyrolytic turbostratic carbon; a resorbable cap obtained with a PGA fiber fabric, the base and the cap being connected with each other along respective edges, to define a closed enclosure; the base is connectable to the urethra and to the ureters of a patient; the base also being of substantially triangular form.

Abstract: A prosthetic implant includes an anterior surface, configured for at least partial contact with an underside of a patient's facial soft tissue. A posterior surface is oppositely placed to the anterior surface. The posterior surface is configured for at least partial contact with a patient's facial bony tissue when the anterior surface is in at least partial contact with the patient's facial soft tissue. An implant body is defined by the anterior and posterior surfaces and extends transversely therebetween. A selected portion of the posterior surface has a texture that mechanically differs from a texture of a majority of the anterior surface.

Abstract: Embodiments of the invention provide compositions include bio degradable polymers, medical implants fabricated from these compositions and methods of using such implants. Many embodiments provide medical implants including a first polymer backbone having a first rate of biodegradation and a second polymer backbone having a second rate of biodegradation faster than the first rate. In some embodiments, the second backbone is configured to be replaced by a natural tissue layer. The first backbone provides a scaffold for the implant while the second backbone degrades. This scaffold can enhance mechanical properties of the implant including various aspects of mechanical strength such as tensile, bending, hoop and yield strength; and elasticity. The scaffold also serves to maintain a minimum level of structural support of the implant during the period of degradation of the second backbone or for the entire life of the implant so that the implant does not mechanically fail.