Abstract: Permanent magnets are implanted in bone to unload compressive forces at joints using the repulsive force therebetween. A porous metal container is implanted first and becomes fixed in place by bone growth. The permanent magnet is then inserted in the container and retained in place. A magnet prescription system includes a display and input device which enables a user to alter parameters such as magnet size, strength and placement and calculate and display the repulsive force that will result.

Abstract: A modular acetabular anti-protrusio cage and acetabular cup combination includes an acetabular cup having a bone ingrowth-promoting surface and a shaped anti-protrusio cage having one or more fixation flanges. The acetabular cup is attached to acetabular bone, and the anti-protrusio cage is thereafter mounted to the inner surface of the acetabular cup. Alternatively, the anti-protrusio cage can be mounted to the inner surface of the acetabular cup before the acetabular cup is attached to acetabular bone. The flanges of the anti-protrusio cage are joined to the ilium, ischium and/or pubis to secure the acetabular cup and the anti-protrusio cage to the hip bone and to distribute forces away from the medial wall of the acetabulum. After the cup and the cage are mounted in the patient, a bearing insert is secured within the interior of the anti-protrusio cage, and a prosthetic femoral head is positioned in the bearing insert.

Abstract: A permanent magnet housed in a porous metal container is implanted in the pelvis of a subject and a second permanent magnet is attached to a supporting structure, such as the seat of a wheelchair. The opposing force produced by the two magnets when the subject rests on the supporting structure reduces the compressive force acting on the tissues therebetween.

Abstract: A prosthetic implant having a fixation stem with varying stiffness is disclosed. The stem comprises an elongated core and segments extending outward from the core. The segments are spaced apart so as to define transverse grooves surrounding the core between adjacent segments. The longitudinal length of the grooves, and the materials used for the core and the segments are selected such that the stiffness of the stem varies from the proximal end to the distal end. Typically, the stiffness of the stem will be lower at the distal end such that the distal end of the stem bears less force when loaded and thereby transfers more load to the proximal end of the stem, which has a higher stiffness. As a result, stress shielding, in which the load bypasses the proximal end of the stem, is minimized and bone resorption adjacent the proximal end of the stem is decreased.

Abstract: A femoral augment, or set of augments, for use with a knee joint prosthesis, where the femoral augment includes a main body portion, an aperture formed within the main body portion and extending in a generally distal/proximal direction, and a pair of legs extending outwardly from said main body portion in a generally posterior direction. In the preferred embodiment, the aperture is configured to receive a stem extension implant, and to allow it to pass through. Additionally, the legs of the femoral augment are preferably configured to be seated proximal of a proximal side of a pair of condylar portions of a femoral component of a knee joint prosthesis. The present invention is intended for situations in which the distal portion of the femur is defective, and it provides a method and devices that allow for preservation of healthy peripheral bone, while still providing the necessary augmentation to the distal portion of the femur.

Abstract: A tibial augment for use with a knee joint prosthesis, composed of annular members of different stock sizes, each size being configured to fit within a cavity formed in a human tibia. The augment may include a stepped distal surface. A provisional (temporary) tibial augment used to ensure a proper fit for the permanent augment is also provided. The provisional may include grooves configured to cooperate with a set of ribs on a tong-like holder used for removing the provisional from the cavity. A pusher for use implanting the tibial augment is also provided. In addition, a system for creating a cavity in a human tibia is also described. The system preferably includes a guide with a slot therein and a set of osteotomes that are inserted within different portions of the slot. Methods for using the tools and/or implanting the prosthetic devices discussed above are also described.

Abstract: A prosthesis for implanting into a bone having a cavity is disclosed. The prosthesis comprises a body and a stem. A first coating including a bone ingrowth promoting material that promotes ingrowth of bone onto the stem and a bioabsorbable material that delays the ingrowth of bone onto the stem is disposed on a proximal portion of the stem outer surface. A second coating including the bone ingrowth promoting material and the bioabsorbable material is disposed on a distal portion of the stem outer surface. The ratio of bone ingrowth promoting material to bioabsorbable material in the first coating is greater than the ratio of bone ingrowth promoting material to bioabsorbable material in the second coating whereby the affixation of the bone to the proximal zone of the stem is faster and stronger over time than the affixation of the bone to the distal zone of the stem.

Abstract: A prosthetic implant having a fixation stem with varying stiffness is disclosed. The stem comprises an elongated core and segments extending outward from the core. The segments are spaced apart so as to define transverse grooves surrounding the core between adjacent segments. The longitudinal length of the grooves, and the materials used for the core and the segments are selected such that the stiffness of the stem varies from the proximal end to the distal end. Typically, the stiffness of the stem will be lower at the distal end such that the distal end of the stem bears less force when loaded and thereby transfers more load to the proximal end of the stem, which has a higher stiffness. As a result, stress shielding, in which the load bypasses the proximal end of the stem, is minimized and bone resorption adjacent the proximal end of the stem is decreased.

Abstract: A permanent magnet housed in a porous metal container is implanted in the pelvis of a subject and a second permanent magnet is attached to a supporting structure, such as the seat of a wheelchair. The opposing force produced by the two magnets when the subject rests on the supporting structure reduces the compressive force acting on the tissues therebetween.

Abstract: Permanent magnets are implanted in bone to unload compressive forces at joints using the repulsive force therebetween. A porous metal container is implanted first and becomes fixed in place by bone growth. The permanent magnet is then inserted in the container and retained in place. A magnet prescription system includes a display and input device which enables a user to alter parameters such as magnet size, strength and placement and calculate and display the repulsive force that will result.

Abstract: A modular acetabular anti-protrusio cage and acetabular cup combination includes an acetabular cup having a bone ingrowth-promoting surface and a shaped anti-protrusio cage having one or more fixation flanges. The acetabular cup is attached to acetabular bone, and the anti-protrusio cage is thereafter mounted to the inner surface of the acetabular cup. Alternatively, the anti-protrusio cage can be mounted to the inner surface of the acetabular cup before the acetabular cup is attached to acetabular bone. The flanges of the anti-protrusio cage are joined to the ilium, ischium and/or pubis to secure the acetabular cup and the anti-protrusio cage to the hip bone and to distribute forces away from the medial wall of the acetabulum. After the cup and the cage are mounted in the patient, a bearing insert is secured within the interior of the anti-protrusio cage, and a prosthetic femoral head is positioned in the bearing insert.

Abstract: An automobile airbag deactivation system is provided to enable emergency services personnel to prevent uninflated airbags from inflating when crash victims are being extricated from crashed automobiles. The system would enable emergency services personnel to deactivate all airbag inflation systems. The airbag deactivation system includes an interrupt switch and a switch control. The interrupt switch is located so as to prevent airbag inflation, such as between the airbag control circuitry and the airbag actuator or between the airbag actuator and the airbag. The switch control includes a device to open the interrupt switch and an access control device. The access control device prevents deactivation of the airbag inflating system by non-emergency personnel. Embodiments of the access control device include restricted electromagnetic band communication between a signal source and a signal transducer. The transducer opens the interrupt switch to deactivate the airbag inflation system.

Abstract: A prosthetic system that includes a prosthetic implant and a support structure secured to an inner surface of the cavity in the end of the bone is disclosed. The support structure defines a channel that extends through the length of the support structure. The prosthetic implant is received in the channel, and a portion of the prosthetic implant is secured to an inner surface of the channel by an adhesive. The stem of the prosthesis beyond the channel may be cemented or uncemented. The support structure may have an approximately funnel shape. The support structure may be a hollow porous cylindrical sleeve. The support structure may comprise a pair of partially hemispherical components arranged in spaced apart relationship thereby defining a channel between the pair of components. The support structure may comprise a plurality of pedestals secured to the inner surface of the cavity of the bone.

Abstract: A prosthesis for implanting into a bone having a cavity is disclosed. The prosthesis comprises a body and a stem. A first coating including a bone ingrowth promoting material that promotes ingrowth of bone onto the stem and a bioabsorbable material that delays the ingrowth of bone onto the stem is disposed on a proximal portion of the stem outer surface. A second coating including the bone ingrowth promoting material and the bioabsorbable material is disposed on a distal portion of the stem outer surface. The ratio of bone ingrowth promoting material to bioabsorbable material in the first coating is greater than the ratio of bone ingrowth promoting material to bioabsorbable material in the second coating whereby the affixation of the bone to the proximal zone of the stem is faster and stronger over time than the affixation of the bone to the distal zone of the stem.

Abstract: An automobile airbag deactivation system is provided to enable emergency services personnel to prevent uninflated airbags from inflating when crash victims are being extricated from crashed automobiles. The system would enable emergency services personnel to deactivate all airbag inflation systems. The airbag deactivation system includes an interrupt switch and a switch control. The interrupt switch is located so as to prevent airbag inflation, such as between the airbag control circuitry and the airbag actuator or between the airbag actuator and the airbag. The switch control includes a device to open the interrupt switch and an access control device. The access control device prevents deactivation of the airbag inflating system by non-emergency personnel. Embodiments of the access control device include restricted electromagnetic band communication between a signal source and a signal transducer. The transducer opens the interrupt switch to deactivate the airbag inflation system.

Abstract: An automobile airbag deactivation system is provided to enable emergency services personnel to prevent uninflated airbags from inflating when crash victims are being extricated from crashed automobiles. The system would enable emergency services personnel to deactivate all airbag inflation systems. The airbag deactivation system includes an interrupt switch and a switch control. The interrupt switch is located so as to prevent airbag inflation, such as between the airbag control circuitry and the airbag actuator or between the airbag actuator and the airbag. The switch control includes a device to open the interrupt switch and an access control device. The access control device prevents deactivation of the airbag inflating system by non-emergency personnel. Embodiments of the access control device include restricted electromagnetic band communication between a signal source and a signal transducer. The transducer opens the interrupt switch to deactivate the airbag inflation system.