A knee joint endoprosthesis apparatus includes a tibial component for anchoring to a tibia and a meniscal component. The tibial component and the meniscal component are coupled to one another in a coupling position and are completely separated from one another in a separating position. The tibial component has a top side defining an abutment plane, against which a bottom side of the meniscal component abuts in the coupling position. The knee joint endoprosthesis apparatus also includes a coupling device for coupling the tibial component and the meniscal component in the coupling position. The knee joint endoprosthesis apparatus is transferrable from the separating position into the coupling position by a relative movement of the tibial component and the meniscal component.

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

An implantable orthopedic knee prosthesis includes a component that is configured to be coupled to a surgically-prepared bone. A fixation side of the component includes a fixation surface that has an angled cement pocket formed therein.

A method of joint arthroplasty includes obtaining an image of at least a portion of the tibial plateau. An outer periphery of at least a portion of the tibial plateau is derived based, at least in part, on the image. An implant is provided for the tibial plateau, the implant having a periphery that includes an outer edge that substantially matches the derived outer periphery of the tibial plateau.

The present disclosure is directed to orthopedic implants and methods of rapid manufacturing orthopedic implants using in vivo data specific to an orthopedic implant or orthopedic trial. Specifically, the instant disclosure utilizes permanent orthopedic implants and orthopedic trials (collectively, “implants”) outfitted with kinematic sensors to provide feedback regarding the kinematics of the trial or implant to discern which implant is preferable, and thereafter rapid manufacturing the implant.

An orthopaedic knee prosthesis includes a femoral component which exhibits enhanced articular features, minimizes removal of healthy bone stock from the distal femur, and minimizes the impact of the prosthesis on adjacent soft tissues of the knee.

In an artificial knee joint implant, an increase in constraint force of a femur component and a tibia component in the anterior-posterior direction and the left-right direction of a patient is enabled, and an increase in an allowable degree of medial pivot motion is enabled. An artificial knee joint implant has a femur component to be fixed to a distal portion of a femur of a patient, and a tibia component to be fixed to a proximal portion of a tibia of the patient. Femur sliding faces of the femur component and tibia sliding faces of the tibia component each include a region in which the curvature radius varies in a predetermined direction.

A method for performing a surgical procedure on a patient using a robotic system and a navigation system. The robotic system includes a cutting tool. The navigation system has at least one locating device to track a portion of the patient during the surgical procedure. The navigation system provides information as to a position of the portion of the patient. An optical cutting guide is projected onto the portion of the patient to enable cutting of the portion of the patient with the cutting tool of the robotic system while the optical cutting guide is projected onto the portion of the patient.

A method for preparing a first bone for receiving a prosthesis. The method includes coupling a revision alignment member to a template; positioning an offset alignment bushing relative to the revision alignment member; positioning the offset alignment bushing at the first bone such that an intramedullary member seated in the first bone extends through a passage defined by the offset alignment bushing; replacing the offset alignment bushing with a first bone cutting bushing; cutting the first bone using the first bone cutting bushing as a guide; replacing the first bone cutting bushing with an offset second bone cutting bushing; providing the second bone cutting bushing with a rotational orientation corresponding to a rotational orientation of the offset alignment bushing; and cutting the first bone using the offset second bone cutting bushing as a guide to prepare the bone to receive an offset prosthesis adapter.

An orthopedic tibial prosthesis includes a tibial baseplate sized and shaped to cover substantially all of a resected proximal tibial surface, and a tibial bearing component sized to leave a posteromedial portion of the tibial baseplate exposed when the tibial bearing component is mounted to the baseplate. The exposed posteromedial portion of the tibial baseplate includes a chamfered profile which cooperates with a correspondingly chamfered profile at a posteromedial edge of the tibial bearing component to create a substantially continuous chamfer extending from the resected tibial surface to the medial articular surface of the tibial bearing component. Advantageously, this chamfer leaves an absence of material (i.e., a relief or void) at the posteromedial edge of the tibial prosthesis, thereby enabling deep flexion of the prosthesis without impingement between the tibial prosthesis and adjacent anatomic tissues or prosthetic structures.