Abstract: A surgical or arthroscopic method for resurfacing at least one surface of a hip joint of a human patient, using a medical device comprising an artificial hip joint surface, wherein the hip joint surface comprising an acetabulum surface and a caput femur surface, said method comprising the steps of: creating at least one hole passing into the hip joint, dissecting and preparing the hip joint, introducing at least one artificial hip joint surface, comprising at least one of an artificial acetabulum surface and an artificial caput femur surface, wherein said at least one artificial hip joint surface, comprising a first sealing member, creating a sealed hollow space between said first sealing member and one of the acetabulum surface or said artificial acetabulum surface and one of the caput femur surface or said artificial caput femur surface, selecting at least one artificial hip joint surface and injecting a material into said hollow space.

Abstract: An implantable medical device, for implantation in a mammal knee joint, comprising an artificial contacting surface adapted to replace at least one contacting surface of the knee joint and to be lubricated when implanted in said joint. The medical device further comprises a reservoir comprising a movable wall portion defining the volume of the reservoir, at least one inlet adapted to receive a lubricating fluid from the reservoir, at least one channel at least partly integrated in said artificial contacting surface, wherein the channel is fluidly connected with said at least one inlet for distributing said lubricating fluid to the surface of said artificial contacting surface.

Abstract: A method of treating a hip joint of a human patient using a pelvic drill comprising a driving member, a bone contacting and an operating device for operating said driving member. The method comprise the steps of cutting the skin of the human patient, dissecting an area of the pelvic bone on the opposite side from the acetabulum, creating a hole in said dissected area using said pelvic drill, said hole passing through the pelvic bone and into the hip joint of the human patient, and providing at least one hip joint surface to the hip joint, through said hole in the pelvic bone of the human patient. In one embodiment the method includes inserting a needle or tube like instrument into the patient's body for filling a part of the patient's body with gas and thereby expanding a cavity within the body.

Abstract: An implantable medical device for lubrication of a synovial joint having a joint cavity is provided. The implantable device comprises a solid lubricant and a feeding device, wherein said feeding device is adapted to feed said solid lubricant into the joint cavity for lubricating the synovial joint.

Abstract: An implantable medical device for implantation in a mammal joint having at least two contacting surfaces is provided. The medical device comprises; an artificial contacting surface adapted to replace at least the surface of at least one of the mammal's joint contacting surfaces, wherein the artificial contacting surface is adapted to be lubricated, when implanted in said joint. Furthermore the medical device comprises at least one inlet adapted to receive a lubricating fluid from a reservoir, at least one channel at least partly integrated in the artificial contacting surface in connection with the at least one inlet for distributing the lubricating fluid to the surface of the artificial contacting surface. The medical device could be adapted to be operable by an operation device to receive the distributed lubricated fluid from a reservoir.

Abstract: Medical devices are provided, comprising a medical device and a sensor.

Abstract: A surgical or arthroscopic method for resurfacing at least one surface of a hip joint of a human patient using a medical device comprising a first sealing member. The hip joint has an acetabulum surface and a caput femur surface and the method comprises the steps of creating at least one hole passing into the hip joint, placing the first sealing member between the acetabulum surface and the caput femur surface, thereby creating a sealed hollow space between the acetabulum and the caput femur using the first sealing member, and injecting a material into the sealed hollow space, and thereby creating an artificial hip joint surface.

Abstract: A protective cover for a prosthetic implant is a flexible body defining an interior space in which a prosthetic implant is receivable. The body includes a lip and an area of weakness formed in one side of the body extending from the lip to a central (i.e., top) portion of the body. The cover can also include an elongated tab extending from a side of the body opposite the slit. The cover covers an exterior surface of the implant when the implant is received in the interior space and thereby prevents soft tissues through which the implant is advanced during surgical introduction of the implant into a joint of patient from contacting and becoming adherent to the exterior surface of the implant. The cover can be extracted and the implant released from the interior space through the area of weakness and into the joint by applying a pulling force to a side of the body opposite the area of weakness.

Abstract: The disclosure is directed to a resilient implant for implantation into human or animal joints to act as a cushion allowing for renewed joint motion. The implant endures variable joint forces and cyclic loads while reducing pain and improving function after injury or disease to repair, reconstruct, and regenerate joint integrity. The implant is deployed in a prepared debrided joint space, secured to at least one of the joint bones and expanded in the space, molding to surrounding structures with sufficient stability to avoid extrusion or dislocation. The implant has opposing walls that move in varied directions, and an inner space filled with suitable filler to accommodate motions which mimic or approximate normal joint motion. The implant pads the damaged joint surfaces, restores cushioning immediately and may be employed to restore cartilage to normal by delivering regenerative cells.

Abstract: An implantable medical device for implantation in a mammal joint having at least two contacting surfaces is provided. The medical device comprises; an artificial contacting surface adapted to replace at least the surface of at least one of the mammal's joint contacting surfaces, wherein the artificial contacting surface is adapted to be lubricated, when implanted in said joint. Furthermore the medical device comprises at least one inlet adapted to receive a lubricating fluid from a reservoir, at least one channel at least partly integrated in the artificial contacting surface in connection with the at least one inlet for distributing the lubricating fluid to the surface of the artificial contacting surface. The medical device could be adapted to be operable by an operation device to receive the distributed lubricated fluid from a reservoir.

Abstract: A prosthetic joint (100) comprises a first component (110) having a first interface portion (111). The prosthetic joint (100) further comprises a second component (120) having a second interface portion (121) with a textured surface (122) to interface with the first interface portion (111) and form a skeletal joint. The textured surface (122) can include a plurality of concave features (123). Each or the concave features (123) can be configured to compress a lubricant (140) to facilitate hydrodynamic lubrication between the first and second interface portions (111, 121) to minimize wear between the first interface portion (111) and the second interface portion (121) of the prosthetic joint (100).

Abstract: A bionic joint device with closed lubrication comprises a main body bionic bone (1), a driven bionic bone (4), an elastic easily-stretching cavity housing (2), a cavity sealing hoop (3), an elastic shock-proof material (5), a high-strength wear-resistant self-lubricating material (6) and a powerful inelastic limit connection (7). The elastic easily-stretching cavity housing (2) is internally filled with lubricating grease (8). The device is applicable to the robotics field and the artificial joint field.

Abstract: Prosthetic artificial joints are described, including hip, knee and shoulder joints.

Abstract: Artificial joint prostheses, including hip, knee and shoulder joints, are described. In some aspects, an artificial joint prosthesis includes: a bone-facing surface of an artificial joint prosthesis, the bone-facing surface configured to face a bone-prosthesis interface in vivo; a non-contact surface of the artificial joint prosthesis, the non-contact surface adjacent to the bone-facing surface of the artificial joint prosthesis; at least one fluid deflection structure attached to the non-contact surface, the fluid deflection structure positioned to direct a flow of synovial fluid away from the bone-prosthesis interface in vivo; and at least one particle retaining structure positioned to contact the directed flow of synovial fluid and configured to retain particles present within the synovial fluid.

Abstract: An acetabular implant cup insert for a joint prosthesis, the insert being of the type having a metal shell (1) and a polymer lining (14) lining the inside space (4) of the shell (1), a receptacle (18) for a prosthetic head being formed in the lining (14), the shell presenting on its inside space (4) elements for preventing the lining (14) being extracted from the shell (1) and elements for preventing the lining (14) turning in the shell (1), the insert being characterized in that the elements for preventing the lining being extracted include a stud (11) disposed on the end wall (10) of the shell (1) and presenting at least one groove (12) or lip. An acetabular implant including a cup and an insert of the above type. A joint prosthesis of the type including an acetabular implant of the above type and a prosthetic head.

Abstract: A pre-assembled orthopaedic implant adapted for improved gas sterilization. The implant includes a first component adapted for assembly with a second component such that a mating surface of the first component is in close proximity with a mating surface of the second component. At least one gas conduit associated with the mating surface of the first component facilitates a sterilizing gas to penetrate into and dissipate from the interface defined by the mating surfaces.

Abstract: A pre-assembled orthopaedic implant adapted for improved gas sterilization. The implant includes a first component adapted for assembly with a second component such that a mating surface of the first component is in close proximity with a mating surface of the second component. At least one gas conduit associated with the mating surface of the first component facilitates a sterilizing gas to penetrate into and dissipate from the interface defined by the mating surfaces.

Abstract: A prosthetic orthopaedic head has a fluid chamber defined therein. A fluid filter is positioned in the fluid chamber. In response to a load being exerted on the prosthetic head, synovial fluid is advanced through a filter thereby removing debris from the synovial fluid. A method of operating a prosthesis is also disclosed.

Abstract: A prefabricated joint is employed for the prosthetic joint. The joint includes prefabricated socket, ball, and capsule. The capsule is attached from the ball to the socket. The capsule seals the area between the ball and socket and prevents wear debris from entering the body cavity. In the case of the hip joint, the doctor need only attach the prefabricated unit to the femoral unit to connect the prosthetic joint after the prefabricated unit and femoral unit have been placed into the acetabular and femur, respectively.

Abstract: A prosthetic orthopaedic head has a fluid chamber defined therein. A fluid filter is positioned in the fluid chamber. In response to a load being exerted on the prosthetic head, synovial fluid is advanced through a filter thereby removing debris from the synovial fluid. A method of operating a prosthesis is also disclosed.

Abstract: An artificial hip joint assembly comprising a femoral component with a stem for being anchored in the medullary space of a femur and a head on the distal end of the stem, an acetabular component for being anchored in the pelvic bone with an acetabular cup which pivotedly supports the head of the femoral component, and an articular capsule made of a flexible material, which is located at the femoral component at one end and at the acetabular component at the other end so as to allow the head to move in the acetabular cup and to prevent wear debris from the bearing zone of the head in the acetabular cup from migrating to the outside.

Abstract: A hip replacement system including a socket having generally hemispherical cavity therein, a ball member cantably affixed within the socket, a stem affixed to the ball member and extending outwardly therefrom, and a lubricant located within a channel formed interior of the stem. The exterior surface of the ball member has at least one opening therein communicating with channel of the stem. The lubricant fills a space between the exterior surface of the ball member and the inner wall of the cavity of the socket. The lubricant is compressed body fat. An inlet is connected to the channel so as to extend outwardly of the stem for allowing the introduction of the lubricant into the channel.

Abstract: A hip replacement system including a socket having generally hemispherical cavity therein, a ball member cantably affixed within the socket, a stem affixed to the ball member and extending outwardly therefrom, and a lubricant located within a channel formed interior of the stem. The exterior surface of the ball member has at least one opening therein communicating with channel of the stem. The lubricant fills a space between the exterior surface of the ball member and the inner wall of the cavity of the socket. The lubricant is compressed body fat. An inlet is connected to the channel so as to extend outwardly of the stem for allowing the introduction of the lubricant into the channel.

Abstract: A joint prosthesis assembly includes a stem for disposition in a canal of a first bone constituting a first portion of the joint, a neck fixed to the stem, a collar fixed on the neck and having a peripheral groove, and an articulating head fixed on the neck. The assembly further includes a cup for disposition in a second bone constituting a second portion of the joint, an insert disposed in the cup to provide an interior lining for the cup, the insert being configured to receive the articulating head for movement therein, and the insert having a peripheral groove therein. A sleeve-shaped membrane is provided with a first O-ring fixed thereto at a first end thereof for disposition in the insert groove, and a second O-ring fixed thereto at a second end thereof for disposition in the collar groove. The membrane is thereby disposed to capture particulate debris generated by the articulating head in the insert. There is further contemplated a method for installing the assembly.

Abstract: An artificial joint system is provided herein. The system includes an artificial joint implantable within an individual, the artificial joint including artificial joint members each having an articulating surface and a bone attachment surface, wherein the articulating surfaces are in articulative engagement therebetween. The system further includes a detection system implanted within, or attached to, the artificial joint members and/or the bones to which the members are attached. The detection system serves for communicating an information signal receivable outside the body, the information signal indicative of a parameter associated with displacement between an artificial joint member and a bone to which it is attached and/or to wear or relative displacement of the articulating surfaces.