1228 results about "Socket hip" patented technology

An implant is formed of an expandable material. An opening is formed in a bone in a patient's body. At least a portion of the implant is positioned in the opening in the bone in the patient's body. The implant is retained against movement relative to the bone in the patient's body by absorbing body fluid with the implant and expanding the implant while the implant is disposed in the opening in the bone in the patient's body. The implant may be a hip replacement member.

An improved hip prosthesis includes an acetabular cup bearing component constructed from a relatively hard and high strength ceramic material for articulation with a ball-shaped femoral head component which may be constructed from a compatible ceramic or metal material. In one form, the acetabular cup further includes a ceramic porous bone ingrowth surface adhered thereto for secure ingrowth attachment to natural patient bone.

The present invention relates in certain embodiments to components of a hip-joint prosthesis. More particularly, embodiments of the invention relate to a leaf-like femoral shaft for use as part of a hip-joint prosthesis, and instruments (e.g., a rasp) and methods for implanting the shaft. The shaft includes an anchoring section extending between a proximal region and a distal end of the shaft. The shaft has a cross-sectional contour that defines a lateral side, a medial side, an anterior side and a posterior side. A corresponding rasp is preferably provided for each femoral shaft. The rasp is inserted into the femur to form a cavity having generally the same configuration as the rasp. The shaft is configured to be over-dimensioned in at least one of the anterior-posterior direction and medial-lateral direction relative to the rasped femur cavity. In one embodiment, the distance between diagonally opposite corner junctions of the shaft is substantially equal to the distance between corresponding diagonally opposite corner junctions of the femur cavity, so as to inhibit excess stress on the corticalis.

This prosthesis comprises a humeral or femoral component and an intermediate component. The concave surface of articulation of the humeral or femoral component is formed by a plate connected by a neck to a part of this component adapted to be anchored in the humeral or femoral medullary cavity. The intermediate component is provided with a member for retaining the humeral or femoral component in a position where the plate is in abutment against the first convex surface of the intermediate component. The retaining member defines a non-circular passage in which the neck is adapted to be displaced as a function of the movements of the humeral or femoral component with respect to the other components of the prosthesis. The retaining member defines with the first convex surface of articulation of the intermediate component a volume for receiving a part of the plate projecting radially with respect to the neck.

A method of determining the voltage and current required for the application of specific and selective electric and electromagnetic signals to diseased articular cartilage in the treatment of osteoarthritis, cartilage defects due to trauma or sports injury, or used as an adjunct with other therapies (cell transplantation, tissue-engineered scaffold, growth factors, etc.) for treating cartilage defects in the human hip joint and a device for delivering such signals to a patient's hip. Anatomic, analytical, and planar circuit models are developed to determining the impedances, conductivities, and current flows in the human hip joint and its surrounding soft tissues and skin that are required to produce a 20 mV / cm electric field in the synovium and articular cartilage of the human hip. The voltage of the signal applied to the surface electrodes or to a coil(s) or solenoid is varied based on the size of the hip joint; larger hip joints require larger voltages to generate the effective electric field.

An intramedullary implant for mounting within an intramedullary canal of a bone is disclosed. The intramedullary implant includes a lower stem portion, an upper stem portion, and a modular sleeve body. The modular sleeve body is connected to one of the lower stem portion or the upper stem portion. The sleeve body includes an inner portion that covers at least a segment of the upper stem portion and has one or more longitudinally extending bone engagement members for engagement with the bone.