Abstract: Surgical devices such as implants or suture fastenings are assembled from a plurality of discrete components, one of which components includes a heat bondable plastic material for bonding the components together. At least two components are bonded to each other by the applying heat to the heat bondable plastic material of one component. The heat bondable plastic material is preferably a polymeric or composite material suitable for surgical applications and implantation in humans, and may be a biodegradable material. A laser may be used as the heat source. The present invention is advantageously embodied in heat bonded fastenings for sutures or K-wires, in which a variety of different suture anchors are usable, including expandable distal suture anchors.

Abstract: A prosthetic medical device exhibiting improved wear resistance is fabricated by sealing at least one polyolefinic material in an airtight container and providing an inert atmosphere within the airtight container. The polyolefinic material is exposed to an irradiation source to yield a cross-linked irradiated polyolefinic material. At least one non-irradiated polyolefinic material is blended with the irradiated polyolefinic material, and the prosthetic medical device is formed from the blended material. Selectively cross-linked polymeric compositions may be created by blending a specific amount of cross-linked resins with a specific amount of uncross-linked resins then cured into a polymeric matrix whereby the desired degree or percentage of overall cross-linking is obtained. The polymeric material may then be formed directly into a finished article by injection molding the polymeric material.

Abstract: A kit (10) for use in implanting a stem (12) into a long bone (36) for use in joint arthroplasty is provided. The kit (10) includes a stem (12) for implantation into the long bone (36), a cement restrictor (16), and a quantity of bone cement (20).

Abstract: The present invention is directed to a set of trial prosthesis instrumentation for use in trial fitting of a medical implant such as a femoral hip prosthesis. The two piece set provides a combined bipolar and unipolar trial prosthesis instrumentation and comprises an outer component and a inner component. The outer component comprises an exterior surface characterized by a substantially hemispherical shape to correspondingly mate with a joint socket and an interior surface characterized by a substantially hemispherical shape, and an inner component that comprises an exterior surface that comprises a surface and that is shaped to correspondingly mate with the interior surface of the outer component and an interior surface characterized by a substantially columnar shape that correspondingly mates with a prosthetic stem. Methods of use are also contemplated.

Abstract: The present invention provides an irradiated crosslinked polyethylene containing reduced free radicals, preferably containing substantially no residual free radical. Disclosed is a process of making irradiated crosslinked polyethylene by irradiating the polyethylene in contact with a sensitizing environment at an elevated temperature that is below the melting point, in order to reduce the concentration of residual free radicals to an undetectable level. A process of making irradiated crosslinked polyethylene composition having reduced free radical content, preferably containing substantially no residual free radicals, by mechanically deforming the polyethylene at a temperature that is below the melting point of the polyethylene, optionally in a sensitizing environment, is also disclosed herein.

Abstract: Adjustable prostheses and related methods provide a wide range of adjustment along or about multiple axes. The prostheses and related methods make possible a straightforward, yet robust way of securing, e.g., a humeral head prosthesis in a desired position and maintaining the prosthesis in the desired position during use.

Abstract: A prosthetic implant includes first, second and third components. The first component is configured to be disposed within the acetabulum. The second component is in a load bearing relationship with the first component, and is operable to rotate in a first axis of rotation. The second component is inhibited from movement in a second axis of rotation. The third component is in a load bearing relationship with the second component. The third component is operable to rotate in the second axis of rotation, but is inhibited from movement with the first axis of rotation.

Abstract: A minimally invasive hip replacement surgical procedure that is also tissue preserving is disclosed. By making a superior incision, rather than a posterior incision, neither the posterior hip capsule, nor the gluteus medius or minimus are dissected. This results in improved post-operative results in the form of less dislocations and better healing.

Abstract: Star polymers of soft segment forming monomers are useful in forming surgical devices. The star polymers can be endcapped with isocyanate, mixed with a filler and/or cross-linked. The polymer compositions are useful, for example, as fiber coatings, surgical adhesives or bone putty, or tissue growth substrate.

Abstract: The present invention is a specialized orthopedic implant having an exterior surface for engaging bone. The surface comprises arrayed projections having at least one forward facing facet directed at least in part toward the leading end of the implant and at least one rearward portion directed at least in part toward the opposite trailing end of the implant. Each of the forward facet and rearward portion has a length and a slope. The length of the forward facet is longer than the length of the rearward facet. The slope of the rearward facet is steeper than the slope of the forward facet. The surface projections also have opposed side facets directed generally toward the sides of the implant. The side facets are located between the forward facet and rearward facet and converge toward each other in a direction away from the base of the surface projections. The surface may also include projections having left and right forward side facets and a rearward facet.

Abstract: A method of making a non-modular prosthetic device for a joint arthroplasty. The method comprises molding a polymer interlayer between a porous metal structure and a polymer insert, wherein the insert generally comprises conventional or cross-linked ultra high molecular weight polyethylene (“UHMWPE”).

Abstract: Implantable prostheses fully or partially formed of polymer having a textured or porous outer surface. The surface permits and encourages osteogenesis into the prosthesis and enables it to become firmly and permanently anchored into surrounding bone. The prostheses include a femoral hip stem formed of a metallic core and a polymeric proximal body with a textured or porous surface formed from a laser texturing, machining, or grit blasting.

Abstract: A method and apparatus for performing a minimally invasive total hip arthroplasty. An approximately 3.75-5 centimeter (1.5-2 inch) anterior incision is made in line with the femoral neck. The femoral neck is severed from the femoral shaft and removed through the anterior incision. The acetabulum is prepared for receiving an acetabular cup through the antenor incision, and the acetabular cup is placed into the acetabulum through the anterior incision. A posterior incision of approximately 2-3 centimeters (0.8-1.2 inches) is generally aligned with the axis of the femoral shaft and provides access to the femoral shaft. Preparation of the femoral shaft including the reaming and rasping thereof is performed through the posterior incision, and the femoral stem is inserted through the posterior incision for implantation in the femur.

Abstract: A prosthetic constraining device for use with a hip replacement prosthesis that includes an acetabular cup assembly adapted to be bonded to a patient's pelvis and a femoral stem adapted to be bonded to the patient's femur, where the femoral stem includes a ball component at its proximal end received within the acetabular cup assembly to form a ball joint type coupling, and where the constraining device includes a ring having a central aperture, where the ring is adapted to be mounted to a rim of the acetabular cup assembly so that the femoral stem passes through the central aperture, where the diameter of the central aperture is less than the diameter of the ball component on the proximal end of the femoral stem so that the ring assists in maintaining the ball joint type coupling between the acetabular cup assembly and the femoral stem, and where the ring comprises a biologic material, a biologically reabsorbable material and a combination of biologic, or biologically reabsorbable materials.

Abstract: A prosthetic medical device exhibiting improved wear resistance is fabricated by irradiating at least one polyolefinic material in the presence of an inert atmosphere to yield a cross-linked irradiated polyolefinic material; blending at least one non-irradiated polyolefinic material with the at least one irradiated polyolefinic material, and forming the prosthetic medical device from the blended material. Selectively cross-linked polymeric compositions may be created by blending a specific amount of cross-linked resins with a specific amount of uncross-linked resins then cured into a polymeric matrix whereby the desired degree or percentage of overall cross-linking is obtained. The polymeric material may then be formed directly into a finished article by injection molding the polymeric material.

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 method and apparatus for performing a minimally invasive (i. e., with the wound developed under an incision being substantially the same size as the incision throughout the depth of the wound) total hip arthroplasty. The apparatus includes a provisional femoral head allowing for radial placement thereof on a provisional femoral neck as well as a posterior retractor sleeve for allowing access to a femur through a posterior incision.

Abstract: A modular trial neck segment is utilized for trialing a hip prosthesis for a total hip arthroplasty. The modular trial neck segment is preferably, but not necessarily, utilized for trialing a hip prosthesis for a total hip arthroplasty. The trial neck segment includes a mount attachable to a stem or broach, and a neck that is translatable on the mount for providing various neck offsets with respect to the mount and/or broach. Neck offset is changed via movement of the neck in a single plane of motion. This facilitates the use of the subject invention in minimally invasive arthroplasty wherein working dimensions are small. The present design replicates the biomechanics of the neck region of the implant. The mount and slidable neck provide a plurality of neck offsets and/or neck lengths for trialing a final prosthesis in a single device.

Abstract: A hip implant having two distinct bodies, a neck body and a bone fixation body. The neck body is formed from a solid metal and has an interface for connecting to a femoral ball. The bone fixation body has an elongated shape and is formed as a porous structure that is inserted into an intramedullary canal of a patient.

Abstract: A medical implant made of polymeric material having an increased oxidation resistance is formed by a method including the steps of placing a resin powder in a sealed container. A substantial portion of the oxygen is removed from the sealed contained by either a vacuum, an oxygen absorbent or by flushing with inert gas. The container is then repressurized with a gas such as nitrogen, argon, helium or neon so that long term storage may be possible. On use, the resin in transferred to a forming device which both melts and forms the resin in an oxygen reduced atmosphere to produce a polymeric raw material such as a rod or bar stock. The medical implant is then formed from this raw material annealed and sealed in an airtight package in an oxygen reduced atmosphere. The implant is then radiation sterilized and thereafter annealed in the package for a predetermined time and temperature sufficient to form cross-links between any free radicals in neighboring polymeric chains.

Abstract: The present invention discloses methods for enhancing the wear-resistance of polymers, the resulting polymers, and in vivo implants made from such polymers. One aspect of this invention presents a method whereby a polymer is irradiated, preferably with gamma radiation, then thermally treated, such as by remelting of annealing. The resulting polymeric composition preferably has its most oxidized surface layer removed. Another aspect of the invention presents a general method for optimizing the wear resistance and desirable physical and/or chemical properties of a polymer by crosslinking and thermally treating it. The resulting polymeric compositions is wear-resistant and may be fabricated into an in vivo implant.

Abstract: Prosthetic joints, components for prosthetic joints, superhard bearing and articulation surfaces, diamond bearing and articulation surfaces, substrate surface topographical features, materials for making joints, bearing and articulation surfaces, and methods for manufacturing and finishing the same, and related information are disclosed, including a prosthetic hip joint having a polycrystalline diamond articulation surface and a plurality of substrate layers.

Abstract: A medical prosthesis for use within a body which is formed of radiation treated ultra high molecular weight polyethylene having substantially no detectable free radial. Preferred prosthesis exhibits reduced production of particles from the prosthesis during wear of the prosthesis, and are substantially oxidation resistant. Methods of manufacturing wear resistant medical prosthesis and materials used therein are also provided.

Abstract: The invention is directed to methods for fabricating devices from polymer precursors, along with devices so fabricated. The methods of the invention include the steps of plasma treating a polymer based resin, paste, preform billet, or extrudate, and employing the treated polymer in the fabricated device. According to one embodiment, the fabricated device can include implantable prosthetics such as heart valves, sutures, vascular access devices, vascular grafts, shunts, catheters, single layered membranes, double layered membranes, and the like. Devices fabricated according to one embodiment of the invention include regions having selected porosity, permeability and/or chemistry characteristics.

Abstract: An implantable femoral hip stem having an offset neck extending outwardly from the proximal region of the stem. The neck has two parallel axes that are separated by an offset distance. A first axis is concentric with the distal end of the neck, and a second axis is concentric with the proximal end of the neck. Together, the two axes form an eccentric neck.

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: Method an device for providing information after insertion of a prosthesis in a hip joint comprising prosthesis stem, and a prosthesis cup and based on this information the position of the components of a hip prosthesis is provided. The prosthesis stem and the prosthesis cup or the part of the body in which the prosthesis is provided can include markers that can be shown on an X-ray picture. The X-ray picture is downloaded in an image processing program having assistance lines for determining the position of the prosthesis components. The X-ray picture is downloaded automatically or manually in the image processing program. The assistance lines are brought into coincidence with the images of the markers on the X-ray picture. Thereafter a calculation unit in the image processing unit calculates the angles for the respective prosthesis components.

Abstract: An intramedullary fixation device for use in securing a trial in the medullary canal of a bone to determine the offset and orientation of a prosthetic implant for replacement of a joint articulating surface of the bone is disclosed. The fixation device comprises a body for receiving a trial and a fixation portion for engaging the trial. A system for use in surgical repair of a joint comprising a selection of prosthetic implants of various sizes, a selection of trials of various sizes corresponding to the sizes of the implants, a selection of fixation devices of various sizes corresponding to the sizes of the trials, a trial fixation device driver for inserting the fixation device and attached trial into the canal of a bone, and a trial device extractor for removing the fixation device from the resected bone is disclosed. Methods of using the fixation device and system of the invention are disclosed.

Abstract: Adjustable prostheses and related methods provide a wide range of adjustment along or about multiple axes. The prostheses and related methods make possible a straightforward, yet robust way of securing, e.g., a humeral head prosthesis in a desired position and maintaining the prosthesis in the desired position during use.

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 prosthetic orthopedic implant assembly including an implant body, and an elastomeric cover connected to the implant body by a mechanical fastener.

Abstract: Test prosthesis system (1) for the insertion of a so-called press-fit-effect femur prosthesis for cement-free implantation into a femur bone (2) in a region (3) in which the press fit effect is preferably obtained and which corresponds to a diaphysial region, the height of which differs depending on the morpho type, characterized in that it consists of a set of at least two shafts (4, 5) each of which has a conical distal region (4, 5) with the same cone angle but a different diameter (D) the first conical region with a smaller maximum diameter D having a proximal region congruent to (i.e. overlapping in size and shape) with a distal region of a second conical region of a second shaft with a larger maximum diameter of the conical region.

Abstract: A prosthetic component is configured to have intentional interruptions in an articulating face thereof. The intentional interruptions are configured to yield an optimum contact area or bearing surface, particularly with regard to low wear and greater lubricity through the application of lubrication and contact mechanics theory for the particular prosthetic component. Such optimization is applied to a wide range of prosthetic component sizes of the particular prosthetic component. The optimum range of percentage area of relief or interruptions, defined as a percentage of a baseline uninterrupted bearing surface area to be removed by the features of the interrupted bearing surface configuration is from 0.3% to 73.7% for hard-on-hard bearing components and from 5.7% to 83.2% for polyethylene-on-hard bearing components. The range for both hard-on-hard and polyethylene-on-hard implants translates to a relieved area ranging from 0.3% to 31.

Abstract: A spacing device for supporting a joint adjacent to diseased bone or missing bone tissue, comprising a support piece and a semi-resilient pad. The pad is shaped to cradle and support the healthy bone joint. The reverse side of the pad is fixedly connected to one end of the support piece. The other end of the support piece is shaped to straddle healthy tissue adjacent the damaged area, such as the ilium when supporting a hip joint and is to be fixedly connected to the adjacent healthy tissue, using a suitable mechanism, such as biocompatible Steinman pins. Diseased, damaged, or necrotic tissue can be removed without requiring removal of the natural bone joint. Because the undamaged bone joint is not replaced, the problems commonly experienced during and following bone joint replacement are avoided. In particular, blood loss during surgery, surgical cost, surgical time, and rehabilitation of the patient after surgery is reduced.

Abstract: According to the present invention a prosthetic bearing component is formed from a composite synthetic plastics material comprising an injection molded thermoplastic polymeric matrix reinforced by a pitch based carbon fiber and having a bearing surface which has been machined with a surface roughness with a value less than Ra 2 &mgr;m. Such components have shown superior wear qualities. Preferably the bearing surface shape is machined with tolerances of 0.1 to 0.15 mm. The composite material must be capable of withstanding a radiation value of at least 2.8 Mega Rads (MRad). In components in which the bearing surface is substantially or part spherical a sphericity of 0.3 &mgr;m within a solid angle of 45° is required.

Abstract: A prosthetic constraining device for use with a hip replacement prosthesis that includes an acetabular cup assembly adapted to be bonded to a patient's pelvis and a femoral stem adapted to be bonded to the patient's femur, where the femoral stem includes a ball component at its proximal end received within the acetabular cup assembly to form a ball joint type coupling, and where the constraining device includes a ring having a central aperture, where the ring is adapted to be mounted to a rim of the acetabular cup assembly so that the femoral stem passes through the central aperture, where the diameter of the central aperture is less than the diameter of the ball component on the proximal end of the femoral stem so that the ring assists in maintaining the ball joint type coupling between the acetabular cup assembly and the femoral stem, and where the ring comprises a biologic material, a biologically reabsorbable material and a combination of biologic, or biologically reabsorbable materials.

Abstract: An implant and method for replacement of the proximal portion of a femur, and specifically for replacement of the natural femoral head is provided. The implant includes a body member for insertion, in use, through the natural femoral neck and in substantial alignment therewith; a head member with a spherical portion for engagement with a natural or a prosthetic hip socket; a joining portion for joining the head member to the body member; and a rod for insertion, in use, through the transverse passage of the body member. The rod is designed such that it has a cross-sectional configuration that contacts the cortical surfaces in the bone and inhibits micro-motion within the bone. In addition, the transverse passage of the body member is configured to complement the configuration of the rod such that the need for stabilizing screws toward the distal end of the rod is eliminated when the implant is assembled within the patient.

Abstract: A prosthetic femoral component is located in a prepared socket in a femur which has been resected at a position on the proximal side of its neck and Includes a tapered insert and a proximal head portion. The proximal end of the insert portion is adapted for location in the prepared socket and has a maximum dimension in a plane normal to the distal-proximal axis of the neck which is larger than the minimum dimension of the neck in a parallel plane. The component takes advantage of the bone at the periphery of the socket which enables the insert to be accurately and firmly located in the bone. The presence of the bone at the outer edges of the socket helps to stabilize the component. Preferably the tapered insert portion is flared outwardly in the proximal direction. The tapered insert portion can be dimensioned to pass through the neck of the femur with which it is to be used or it can stop short of it.

Abstract: Regardless of the materials used in an artificial joint component design, the present invention applies gas cluster ion beam (GCIB) technology in order to modify the component's surface(s) so as to increase lubrication between contact surfaces, thereby substantially reducing wear debris, osteolysis complications, and accelerated wear failure. The approach of the surface modification comprises an atomic level surface patterning utilizing GCIB to apply a predetermined pattern to the surface(s) of the joint implant to reduce frictional wear at the interface of the surfaces. A reduction in wear debris by GCIB patterning on any surface(s) of a joint prosthesis reduces accelerated failure due to wear and osteolysis and results in a substantial cost savings to the healthcare system, and reduces patient pain and suffering.

Abstract: A hip assembly and method are described in which a femoral head cap component secured to the femur with at least one screw is engaged with an acetabulum shell component affixed to the acetabulum with at least one screw, and a trochanteric osteotomy plate is secured to the femur with screws. The assembly further includes a psoas recess in the acetabulum shell for allowing freedom of movement of the illiopsoas tendon, countersunk cancellous screws for securing the components to the bones, and fins mounted on the femoral cap to prevent rotation in the bone.

Abstract: A hip joint prosthesis having a retainer for a modular bearing in an acetabular cup and also having a bearing extraction member mounted in the cup for removal of a primary bearing. One embodiment of the bearing extraction member is a plug which is located in a hole provided in the acetabular cup and which is covered by a polyethylene bearing directly molded into the cup. The plug is an internally threaded plug with a convex head and is adapted to be pulled out of its resting position in the cup with the aid of an extraction tool such that the head of the plug exerts a removal force on the molded polyethylene bearing, causing it to disengage from the cup.

Abstract: A joint prosthesis comprising at least a first and a second load carrying member, the first load carrying member being substantially more shock absorbing and resilient than the second load carrying member.

Abstract: Milling tool for emptying the femoral medullary space, while creating a space for the shaft of a hip prosthesis, which comprises a flexible core and a plurality of conical, rotationally symmetrical milling segments, mounted in superimposed manner on the core and provided with a central through-bore, the milling segments being so connected to the core and/or the milling segments adjacent thereto, that a rotational force applied to the core and/or the upper segment is transferred to the individual milling segments, as well as a hip prosthesis with a conically directed shaft and a ball mounted on the proximal end of the shaft and which comprises a flexible core, a plurality of conical, rotationally symmetrically segments, mounted in superimposed manner on the core and provided with a central through-bore and a device for tensioning the core to bring a stiffening of the shaft formed from the individual segments.

Abstract: Methods and compositions for fabricating prosthetic medical devices exhibiting improved wear resistance include selectively cross-linking polymeric resins then curing and shaping the polymer into a finished article. The selectively cross-linked polymeric compositions may be created by blending a specific amount of cross-linked resins with a specific amount of uncross-linked resins then cured into a polymeric matrix whereby the desired degree or percentage of overall cross-linking is obtained. The polymeric material may then be formed directly into a finished article by injection molding the polymeric material.

Abstract: An acetabular alignment method and apparatus utilize natural landmarks available on a pelvis to guide the alignment of an acetabular device in connection with the implant of a prosthetic hip joint at an implant site in the pelvis. The acetabular device is engaged with a positioning shaft having a longitudinal shaft axis, and locators are mounted upon the positioning shaft for placement adjacent selected landmarks on the pelvis to orient the shaft axis relative to the acetabular axis of a prepared acetabulum at the implant site in order to place the shaft axis at a prescribed angle of abduction and a prescribed angle of anteversion, thereby orienting the acetabular device at the appropriate angle of abduction and the appropriate angle of anteversion.

Abstract: Prostheses with artificial joints have only a few metallic and ceramic materials whose compatibility with human or animal tissue has been established. These materials, however, cannot be combined with one another in any manner if a friction pairing occurs as a result, for example, in the case of artificial joints. With artificial joints, joint partners are required to have good mechanical properties as well as tribological properties. According to the invention, a sintered material is thus provided which is comprised of zircon oxide with an addition of 0.1 to 40 wt. % aluminum oxide. This sintered material enables an artificial joint of a prosthesis whose other ceramic materials are comprised of aluminum oxide or zircon oxide with the given proportions of aluminum oxide to be assembled with joint partners.

Abstract: A medical prosthesis for use within the body which is formed of radiation treated ultra high molecular weight polyethylene having substantially no detectable free radicals, is described. Preferred prostheses exhibit reduced production of particles from the prosthesis during wear of the prosthesis, and are substantially oxidation resistant. Methods of manufacture of such devices and material used therein are also provided.

Abstract: The invention relates to a hip joint which has an attachment for an artificial leg and which, in order to permit a largely natural walking movement, has the following features: a front link (5) and a rear link (6) are articulated at their respective upper sections, via a first joint connection (1) and a second joint connection (2), respectively, to a front section and a rear section, respectively, of an upper transverse link (7), and are articulated at their respective lower sections, via a third joint connection (3) and a fourth joint connection (4), respectively, to a front section and a rear section, respectively, of a lower transverse link (8); the first and third joint connections (1, 3) together have at least five degrees of freedom; the second joint connection (2) is a hinge pin which with its pivot axis (2a) is approximately perpendicular to the sagittal plane and has one degree of freedom; the fourth joint connection (4) has a pivot axis (4a) with mediolateral and anteroposterior inclination and with

Abstract: A spacing device for supporting a joint adjacent to diseased bone or missing bone tissue, including a support piece and a semi-resilient pad. The pad is shaped to cradle and support the healthy bone joint. The reverse side of the pad is fixedly connected to one end of the support piece. The other end of the support piece is shaped to straddle healthy tissue adjacent the damaged area, such as the ilium when supporting a hip joint and is to be fixedly connected to the adjacent healthy tissue, using a suitable mechanism, such as biocompatible Steinman pins. Diseased, damaged, or necrotic tissue can be removed without requiring removal of the natural bone joint. Because the undamaged bone joint is not replaced, the problems commonly experienced during and following bone joint replacement are avoided. In particular, blood loss during surgery, surgical cost, surgical time, and rehabilitation of the patient after surgery is reduced.

Abstract: A hip joint socket implant for total hip replacement, can contain a modified surface configuration of its cement-fixable outer wall having small, widely dispersed cement spacer elevation members. The implant has a unique snap-fitted arrangement of the head-restraining marginal outlet of the acetabular component with posterior and anterior cut outs of the implant to avoid premature impingement against a prosthetic femoral neck, allowing a normal, non-dislocating range of unobstructed external and internal rotation of the hip, and a hood that is a marginally extended continuation of the superior one-half or so of the cup containment that is of a sufficient magnitude to reduce the overall dimension of the socket outlet to less than a hemisphere, which is especially pertinent to a conventional hip replacement acetabular cup prosthesis.