A device configured for use as a medical implant is disclosed. The device includes an anchor body including a first end configured to retain an elastic articulating component and a second end including a collar defining a receptacle configured to receive a portion of a fixation element. The fixation element can include a head portion and a threaded portion. The head portion is configured to be inserted and retained within the receptacle and the threaded portion is configured to retain the fixation element within a patient recipient site.

A knee joint prosthesis system for implantation in a first knee joint of a patient. The first knee joint has a condition. The knee joint prosthesis system includes a tibial baseplate component, a femoral component having a femoral articulation surface, and a tibial insert. The tibial insert includes a tibial articulation surface configured to articulate with the femoral articulation surface. The tibial articulation surface includes a medial tibial compartment asymmetrical to a lateral tibial compartment. The tibial articulation surface is shaped to cooperate with the femoral articulation surface to adapt kinematics of the first knee joint having the condition and the tibial articulation surface is also suitable for implantation in a second knee joint on a second side, the second knee joint lacking the condition.

A knee joint prosthesis is configured to move between an extended position and a flexion position. The knee joint prosthesis includes a femoral component configured to be mounted to a femur, and a tibial component configured to be mounted to a tibia. The tibial component is configured to engage the femoral component to form the knee joint prosthesis. A post is fixedly connected to one of the femoral component and the tibial component, and a cam recess is defined on the other of the femoral component and the tibial component. The cam recess is configured to engage the post in either the extended position or the flexion position of the knee joint prosthesis. An artificial ligament is fixedly connected to the femoral component and the tibial component to simulate either an anterior cruciate ligament or a posterior cruciate ligament.

A femoral assembly includes a femoral component that includes condylar portions and an anterior flange portion. The condylar portions and anterior flange portion together define an outer side of the femoral component for articulating with a tibial prosthesis and an inner bone facing side opposite the outer side. The inner bone facing side defines five intersecting component inner surfaces that each extend from a lateral side of the femoral component to a medial side thereof. A femoral augment includes condylar portions and an anterior flange portion. The condylar portions and anterior flange portion together define an outer side of the femoral augment comprised of five intersecting augment outer surfaces and an inner side comprising no more than three intersecting augment inner surfaces. The augment outer surfaces correspond to the component inner surfaces of the femoral component. The augment inner surfaces correspond to resected surfaces of a distal femur.

The joint implant of the present invention is fitted into C1-2 lateral joints through the back of the neck instead of oral approach to avoid infections. It is made of 2 inter-digitating components. One part of the joint implant has a circular railing circumference of a circle, the center of which is odontoid, that inter-digitates in a corresponding circular channel of the other part. Two such implants are fixed on both sides of C1-2 joint simultaneously along the circumference. The circular railings provide mainly circular motion in clockwise and anti-clockwise direction. With some degree of play in channel and rail and making the interacting surfaces of the implant convex on convex, provides the gyroscopic motion with lateral and translational movement and also coupling (vertical translation on rotational movement). This gyroscopic design makes it universal and is likely to work in C1-2 joints of every individual with any possible joint orientation.

A knee joint prosthesis for a tibia and femur can include a tibial component, a tibial bearing, and a post. The tibial bearing can include a first bearing portion, a second bearing portion, and an aperture. The first bearing portion can be positionable on a first side of the sagittal axis and can have a first shape. The second bearing portion can be positionable on a second side can have a second shape different than the first shape. The post, together with the first bearing portion and the second bearing portion, can be configured to promote the femur to pivot substantially about the first bearing portion.

A knee joint prosthesis is capable of moving between an extended position and a flexion position. The knee joint prosthesis includes a femoral component that is configured to be mounted to a femur, and a tibial component that is configured to be mounted to a tibia. The femoral component and the tibial component are at least partially connected together by a geared arrangement.

According to some embodiments of the invention, an intervertebral disc replacement includes a first layer having a lower surface for contacting a first vertebral bone, a second layer coupled to the first layer, the second layer comprising a plurality of compressible column springs, and a third layer coupled to the second layer, the third layer having an upper surface for contacting a second vertebral bone. Each of the plurality of compressible column springs comprises a plurality of stacked coils, and each of the plurality of stacked coils has a spring constant (K). At least one of the plurality of compressible column springs includes a first coil having a first spring constant and a second coil comprising a second spring constant, wherein the first spring constant is different from the second spring constant.

A total knee replacement, comprising a femoral and a tibial component in articulating contact that can restore normal joint function. The articulation between the two components is controlled by four guide surfaces.

According to some embodiments of the invention, an intervertebral disc replacement includes a first layer having a lower surface for contacting a first vertebral bone, a second layer coupled to the first layer, the second layer comprising a plurality of compressible column springs, and a third layer coupled to the second layer, the third layer having an upper surface for contacting a second vertebral bone. Each of the plurality of compressible column springs comprises a plurality of stacked coils, and each of the plurality of stacked coils has a spring constant (K). At least one of the plurality of compressible column springs includes a first coil having a first spring constant and a second coil comprising a second spring constant, wherein the first spring constant is different from the second spring constant.