Abstract: An acetabular spacer device, of a type that is temporary and disposable, adapted to be implanted in use in a bone cavity placed at a joint of the human body, such as a hip or shoulder joint, has a cup-like shape, substantially hemispherical, and includes a first convex surface, adapted to be positioned at the bone cavity, a second concave surface, which defines a cavity, further includes at least one pharmaceutical or medical substance, such as at least one antibiotic, adapted to treat during use an ongoing infection in the bone cavity.

Abstract: A hip implant is provided that includes a metal acetabular cup to be inserted into an acetabulum of the pelvis, a femoral head and neck portion with a polymer femoral head molded onto a metal formal head base that is attached to a metal femoral neck rod configured to be inserted into the neck of a femur, and a metal main body shaft configured to be inserted into a femoral shaft region of the femur and secured by bone screws. The head base may have stabilizing features, such as dimples and peripheral mounds, over which the femoral head is molded. The main body shaft also has diagonal hole located at the center line of the neck of the femur to receive the femoral neck rod at an adjustable angle. The femoral head interfaces with the acetabular cup as a smooth plastic-to-metal spherical-surface joint.

Abstract: A system for shoulder repair includes a prosthetic stemless shoulder implant including a base member extending along a longitudinal axis from a first side to a second side. The second side adapted to engage bone of a patient. The base member defines a hole that extends along the longitudinal axis and through the second side of the base member for receiving a flexible member therethrough. The system includes a fixation construct including a first fixation device and a second fixation device, the first and second fixation devices connected by the flexible member. While the first fixation device is positioned outside of the second side of the base member and the second fixation device is positioned within the base member, the flexible member is adapted to tension the first fixation device with respect to the second fixation device.

Abstract: Systems, devices, and methods are provided for orthopedic implants. The implants may include a base member, such as an acetabular shell or an augment, that is configured to couple with an augment, flange cup, mounting member, or any other suitable orthopedic attachment. An implant may include abuse member that has at least two projections with a gap between the projections. The gap between the projections allows the implant to be implanted around another implanted component, such as around a bone screw of an acetabular shell. The implant may include a fixation element, such as a screw or a cement trough, on one or more projections to couple the implant to an implanted acetabular shell. The implant may also include timing marks to facilitate alignment with corresponding marks on another implanted component.

Abstract: A dynamic porous coating for an orthopedic implant, wherein the dynamic porous coating is adapted to apply an expansive force against adjacent bone so as to fill gaps between the dynamic porous coating and adjacent bone and to create an interference fit between the orthopedic implant and the adjacent bone.

Abstract: A trial device and a method for using the device in surgery are disclosed. The device includes a body including a proximal portion and a distal portion. The proximal portion has a post or trunion projecting therefrom. The distal portion extends from the proximal portion and includes a first arm and a second arm, the first and second arms being movable with respect to one another. The body further includes a cavity formed therein so as to extend through the proximal portion and into the distal portion. The device further includes a driver adapted for sliding engagement within the internal cavity of the body such that movement of the driver, preferably in a distal direction, causes movement of a portion of the first arm away from a portion of the second arm.

Abstract: Methods and apparatuses for attaching tissue structures to orthopaedic implants. In one exemplary embodiment, the methods and apparatuses are used to attach soft tissue and/or bone to a proximal tibial implant. In another exemplary embodiment, the methods and apparatuses are used to attach soft tissue and/or bone to a proximal femoral implant.

Abstract: An orthopaedic prosthesis for use in a hip replacement surgery. The orthopaedic prosthesis includes a metallic foam shell and a metallic core. The metallic core includes a neck configured to receive a femoral head component and a stem extending through the metallic foam shell.

Abstract: A bone implant comprises a core 10 having an integral anchoring structure 12 at its surface. The structure 12 comprises an array of upwardly extending mutually spaced pointed claw-like teeth 14 for digging into bone to which the implant is to be attached, and a network of pores 16 underlying the array and communicating with the exterior of the surface via openings 18 between the teeth, the pores allowing for the circulation of nutrients to promote bone growth.

Abstract: A method for centering a stem of an implant at an implantation site. The method includes implanting at the implantation site the implant having a sleeve rigidly mounted to the stem of the implant, the stem extends through an interior area of the sleeve. The method further includes compressing the sleeve by applying force to the sleeve to expand a mesh portion of the sleeve outward from the stem and into engagement with sidewalls of the implantation site to thereby center the stem at the implantation site.

Abstract: An implant stem (1, 2) for implantation in a femur, comprising: a base portion (3) disposed at the proximal end (4) of the stem and a stem portion (5) extending to the distal end (6) of the stem, wherein the base portion (3) has an engagement means (7) for engaging, in use, with the resected end of the femur. An implant comprising such a stem (1, 2) and a head. A method for implanting such implants in a femur.

Abstract: A method for trochanteric reattachment can include positioning a femoral prosthesis relative to a proximal portion of a femur. A first portion of a self-locking adjustable flexible member construct can be coupled to a first attachment region of the prosthesis, and a second portion of the self-locking adjustable flexible member construct can be coupled to a second attachment region of the femoral prosthesis, where the second portion can be opposite the first portion. A trochanter can be positioned relative to the femur and a trochanteric engaging region of the prosthesis, and the self-locking adjustable flexible member construct can be positioned around an outer surface of the trochanter. Free ends of the self-locking adjustable flexible member construct can be tensioned to draw the trochanter into secure engagement with the prosthesis and the femur via the self-locking adjustable flexible member construct in an absence of a knot.

Abstract: A hip-joint prosthesis includes a shaft which is configured to be inserted into the femur and whose surface has an osteoinductive finish. This finish is provided exclusively in the metaphyseal portion of the shaft and laterally from the line delineating the maximum antero-posterior dimension of the shaft cross section. This ensures a better involvement of the metaphyseal spongiosa in the flow of forces, without compromising the ability to perform follow-up surgery on the prosthesis.

Abstract: A femoral prosthesis. The femoral prosthesis includes an implant body having a proximal end and a distal end and a shoulder at the proximal end, the shoulder being structured and dimensioned for a tight press fit into the neck of a femur. The implant body includes a trunk at the distal end, the trunk having a wedge formed by a tapered portion extending in the direction of the distal end of the implant, body. The implant, body also includes a medial column extending from the shoulder toward the distal end and a lateral column extending from the shoulder toward the distal end. The wedge, the medial column, and the lateral column to provide multi-planar stability for the implant body and surface area for fixation of the implant body.

Abstract: A femoral prosthesis. The femoral prosthesis includes an implant body having a proximal end and a distal end and a shoulder at the proximal end, the shoulder being structured and dimensioned for a tight press fit into the neck of a femur. The implant body includes a trunk at the distal end, the trunk having a wedge formed by a tapered portion extending in the direction of the distal end of the implant body. The implant body also includes a medial column extending from the shoulder toward the distal end and a lateral column extending from the shoulder toward the distal end. The wedge, the medial column, and the lateral column to provide multi-planar stability for the implant body and surface area for fixation of the implant body.

Abstract: A total hip femoral prosthesis provides a shortened neck and high porous coating level. Additionally, a means for strengthening the neck may be incorporated to increase stress transfer to the native bone. A method for reducing potential impingement that results from a high neck resection level includes cutting chamfered surfaces into the bone surrounding the proximal end of the implant. Instrumentation and methods of creating chamfered cuts are disclosed.

Abstract: A joint prosthesis system has a metal shaft, which is implanted in the femur, a throat having an outer cone, a joint ball made of ceramic and an accommodation for the throat. The accommodation has an inner cone, and a sheath-shaped adapter, which is arranged between the shaft and the joint ball in a clamping manner. Due to an exceptional elasticity and a special shaping of an inner and outer wall section of the adapter, the application of force to a narrow surface region on the metal outer cone and the application of the force into the ceramic inner cone is extensively concentrated on a load-bearing region (B) opposite the narrow surface region within the largest mass expansion of the ceramic joint ball.

Abstract: A trial device and a method for using the device in surgery are disclosed. The device includes a body including a proximal portion and a distal portion. The proximal portion has a post or trunion projecting therefrom. The distal portion extends from the proximal portion and includes a first arm and a second arm, the first and second arms being moveable with respect to one another. The body further includes a cavity formed therein so as to extend through the proximal portion and into the distal portion. The device further includes a driver adapted for sliding engagement within the internal cavity of the body such that movement of the driver, preferably in a distal direction, causes movement of a portion of the first arm away from a portion of the second arm.

Abstract: The present invention relates to a hip prosthesis (1) comprising a femoral stem (20) that can be inserted within the medullar channel of a patient femur, the medial side (21) of said femoral stem (20) having, in the proximal portion (40), the shape of an arc, said femoral stem (20) being provided with substantially longitudinal lateral reliefs (60, 61), so that said stem (20) can be fixed to the bone tissue by pressure, and a prosthetic neck (30), provided with means for coupling with a morse cone type spherical head (31), said prosthesis (1) being characterised in that the cross section of said longitudinal reliefs (60, 61) has an apex portion (60?), having the lateral walls included within a first angle (c), and a base portion having the lateral walls included within a second angle (d), which is minor or equal to said first angle (c), and in that grooves (63) are provided between said longitudinal reliefs (60, 61), that can be homogeneously filled with spongious bone tissue.

Abstract: A method for arthroplasty includes using a self-locking prosthesis that has a member structured to transfer a load produced by the weight of a patient to a bone. An expandable bone-locking portion that is integral to the member includes a shape-memory material and expands to produce a locking force. A portion of the bone is removed to form an aperture in the bone. The bone-locking portion is inserted into the aperture, and a temperature increase causes a change from a contracted state to an expanded state resulting in expansion of the bone-locking portion so as to contact the inner surface. The expanding is sufficient to create a locking force at the junction between the inner surface and the bone-locking portion of the prosthesis and the majority of the locking force is applied at or above the metaphysis. The length/width ration of the prosthesis may be less than or equal to 5. The resulting reconstructed long-bone may have improved primary and long-term stability.

Abstract: A method for trochanteric reattachment can include positioning a femoral prosthesis relative to a proximal portion of a femur. A first portion of a self-locking adjustable flexible member construct can be coupled to a first attachment region of the prosthesis, and a second portion of the self-locking adjustable flexible member construct can be coupled to a second attachment region of the femoral prosthesis, where the second portion can be opposite the first portion. A trochanter can be positioned relative to the femur and a trochanteric engaging region of the prosthesis, and the self-locking adjustable flexible member construct can be positioned around an outer surface of the trochanter. Free ends of the self-locking adjustable flexible member construct can be tensioned to draw the trochanter into secure engagement with the prosthesis and the femur via the self-locking adjustable flexible member construct in an absence of a knot.

Abstract: A removable prosthetic element having an elongated stem with a smooth outer surface, a portion of which defines, when the element is implanted in a subject, a contact interface between the stem and surrounding bone and/or fibrous tissue. One or more longitudinal guide channels in the form of longitudinal circular bores are located to the interior of the outer surface of the stem, the bore being adapted for receiving and laterally retaining a drill bit. One or more anchoring cavities comprising pores or passages having an opening with a distal perimeter at the outer surface of the stem lead to a longitudinal guide channel. At least a portion of the distal perimeter is formed as a sharp or pointed cutting edge that cuts the ingrown tissue upon upward removal of the element.

Abstract: A hip-joint prosthesis includes a shaft which is configured to be inserted into the femur and whose surface has an osteoinductive finish. This finish is provided exclusively in the metaphyseal portion of the shaft and laterally from the line delineating the maximum antero-posterior dimension of the shaft cross section. This ensures a better involvement of the metaphyseal spongiosa in the flow of forces, without compromising the ability to perform follow-up surgery on the prosthesis.

Abstract: A hip prosthesis includes a straight shaft which is to be inserted into the femur, the straight shaft including a proximal part that is configured to be inserted in the metaphyseal region of the femur. The proximal part has, on each of its front and rear faces, at least one projecting fin with a steep medial flank that deviates at least over part of its length away from the longitudinal direction of the shaft. At its top the proximal part is inclined toward the femoral neck. In this way, when the shaft is driven into the bone, the bone substance surrounding the fin is compacted and is able to absorb greater forces. The height of the fin decreases from its medial flank toward its lateral edge.

Abstract: A system and method for attaching soft tissue to a prosthetic implant can include a prosthetic component that defines a soft tissue attachment region having an attachment surface thereon. A first construct can be formed of porous metal and be removably coupled to the attachment surface. A second construct can be positioned outboard of the soft tissue. A fastener can be engaged to the second construct and capture the soft tissue against the first construct. The fastener can be coupled on a distal end to the first prosthetic component.

Abstract: A canine femoral stem system provides a set of sizes of stems designed to fit in a reamed femoral bone canal with controlled interference. The canine femoral stems can be implanted using either a cemented or cementless procedures. Cementless stems have a porous coating of sintered beads on the tapered proximal section providing interference with reamed femoral canal causing friction and initial stability. The distal end of the stem has a tapered fit and contacts the lower region of the reamed femoral bone canal due to curvature of the stem providing distal stability. The porous coating encourages bone ingrowth in the cementless system or cement penetration resulting in long term stability. The cementless system uses either cast cobalt chromium stems with 250±50 ?m beads of cobalt chromium or Ti- 6Al- 4V stem with 250±50 ?m beads of chemically pure titanium.

Abstract: The invention relates to an implant system having at least one shaft of a prosthesis, in particular a hip joint prosthesis, which can be anchored without cement, and a set of instruments for the preparation of the bone in which the shaft is to be anchored, wherein the shaft has an arcuate base body with a trapezoidal or rectangular cross-section and the set of instruments includes a first instrument which is shaped in accordance with the arcuate shape of the shaft and with which a recess serving for the reception of the base body can be established in the bone; and wherein the shaft is provided with ribs in the proximal region and the set of instruments includes a guide body shaped in accordance with the arcuate shape of the shaft for a second instrument with which structures can be manufactured in the bone serving to fix a path for the shaft ribs when the guide body is located in the recess.

Abstract: A system and method is provided in which natural bone removed during a joint surgery is retained along with the natural attachment of the associated soft tissues. For instance, in a hip surgery, a portion of the greater trochanter is removed while retaining the soft tissue attachments. An implant and the bone portion are provided with mating features, such as a keystone configuration. The keystone configuration can include mating male and female dovetail configurations. The bone portion can be engaged to the mating feature of the implant to support the natural bone and its soft tissue attachment in an anatomically appropriate position.

Abstract: Leaflike shaft (1) of a hip-joint prosthesis for anchoring in the femur, according to a towards a distal end (5), with a femur-anchoring section (1a, . . . 1i) having a long axis (A) and with a prosthesis neck (2), wherein the femur-anchoring section (1a, . . . 1i) has a substantially rectangular external contour in a plane perpendicular to the long axis (A), optionally with recesses in the side edges and/or at the corners.

Abstract: A trial device and a method for using the device in surgery are disclosed. The device includes a body including a proximal portion and a distal portion. The proximal portion has a post or trunion projecting therefrom. The distal portion extends from the proximal portion and includes a first arm and a second arm, the first and second arms being moveable with respect to one another. The body further includes a cavity formed therein so as to extend through the proximal portion and into the distal portion. The device further includes a driver adapted for sliding engagement within the internal cavity of the body such that movement of the driver, preferably in a distal direction, causes movement of a portion of the first arm away from a portion of the second arm.

Abstract: An external proximal femoral prosthesis for total hip arthroplasty (THA) is described, which fundamentally comprises a shell configured a hollow, thin-wall, asymmetric bell shape and a plurality of tension anchor means. An inner transverse cross contour of the shell forms a cavity, which could be affixable to a profile of outer surface of the area of neck, trochantic bed and calcar of the proximal femur. A neck portion of the shell is compatible with acetabular components (ball and cup). The prosthesis is mechanically fastened by tension anchor means during the operation and further biologically secured by in-growing bone through the side holes on the shell wall and into its interior coating surface of implant wall thereafter. The loading force on the femoral head would be well transferred and distributed on the shell and then directly conducted into the cortical bone of the femoral shaft therearound.

Abstract: Prosthetic hip stems and acetabular cups for use in prosthetic hip joints. The hip stem may include a core having a stem portion and a neck portion, a polymer matrix layer substantially covering the stem portion of the core, and a porous metal layer substantially covering the polymer matrix layer. The polymer matrix layer connects the core and the porous metal layer and provides a stiffness for the hip stem which more closely mimics the stiffness of bone than do known hip stems. The hip stems and acetabular cups additionally include a number of improvements adapted for more optimized results with certain types of patient anatomy, such as the anatomy of female patients, for example.

Abstract: An endoprosthesis utilizes a biomechanical structure based on the lever model of first degree. Contrary to the widespread practice, the inventive structure has a stem placed inside the femur bone, which is not rigidly attached to this bone. Accordingly, the bone, following its known tendency to slightly pivot away from the medial plane of the body in response to the loads, does not directly contact the stem. The neck portion experiences even greater loads then the stem. The supporting anchor has a region extending laterally from the stem and pressing against a supporting surface of the housing, which also extends laterally from the body of the housing. Since the stem, supporting anchor and neck are typically constitute a one-piece component, the lateral surfaces of the supporting anchor and housing are in continuous frictional contact during displacement of the stem and housing relative to one another.

Abstract: The present invention provides a positioner for controlling the position of a femoral hip implant within the intramedullary canal of a femur.

Abstract: The hip-or shoulder-joint endoprosthesis has a stem (10) and a ball head (20) that has an arched top side (21) and a closed underside (22). The longitudinal axis of the stem (10) forms an angle of at most 30° with the axis of the ball head (20). The stem (10) tapers with an overall aperture angle in the range of 5 to 30°. The ball head (20) has the shape of a sphere section of less than a hemisphere. The length of the stem (10) is less than the diameter of the ball head (20). The longitudinal axis of the stem (10) can coincide with the axis of the ball head (20).

Abstract: A fixation device and method for attaching an external prosthesis to a bone. The fixation device includes a main body having a compliant portion operable to be expanded and contracted. The main body has a first end fixedly retained in the bone and a second end coupled to an extension for receiving the external prosthesis. The main body and the extension define respectively first and second engagement surfaces for constraining a bone graft therebetween.

Abstract: A modular prosthesis for replacement of hip joints has a shaft that fits into the femur canal to replace a previous prosthesis, which is made up of sections aligned and held on a cylinder that extends through the sections. In this matter, the length of the shaft can be changed to insure that the shaft will be aligned with bone sections that have not been damaged from the previous prosthesis. The shaft includes a shoulder segment adjacent the proximal end of the femur to attach to ball or head prosthesis using tension carrying screws or elements.

Abstract: A joint prosthesis (10) for cooperation with a long bone (12) and a second bone (26) for use in arthroplasty is provided. A cavity (20) is formed in the long bone (12) and defined by an inner wall (30) of the long bone (12). The prosthesis (10) includes a stem component (32) including a distal portion (34) of the stem component (32) for placement at least partially within the cavity (20) of the long bone (12) and for securing to the long bone (12). The stem component (32) defines a longitudinal axis (36) of the stem component (32). The prosthesis (10) also includes a second component (32) securable to the second bone (26) and for cooperation with the stem component (32). The prosthesis (10) further includes a bearing (40) for placement in the cavity (20) between the stem component (32) and the long bone (12) so that the distal portion of the stem component (32) is spaced from the inner wall (30) of the long bone (12).

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 implant is provided for replacing the articular portion of a bone. The implant includes spaces adjacent bones in articulating relation and threadably anchors the implant to a bone. The threaded anchor permits bone growth axially and transversely therethrough.

Abstract: The specification discloses a modular system for the formation of a prosthesis for the replacement of a long bone in a human or animal body. The system provides a prosthesis comprising a proximal or distal end component such as a trochanter (1) or condylar head, forming one component of a prosthetic joint, a shaft (5) for assembly with the distal or proximal end component and a stem (8) for engagement in a resected bone. The system allows the assembly of a custom fitted prosthesis from a limited range of components.

Abstract: A hip prosthesis constructed to transfer forces to the femur without relative movements that cause failures. The prosthesis stem has an open sided central bore. The proximal end of the prosthesis is configured to seat against interior surfaces of the femoral canal and support a femur head on a prosthesis shoulder that seats on the stem proximal end while maintaining the neck of the femur intact.

Abstract: Prosthetic joint replacement ensemble includes an artificial joint implant component having a non-bone-interfacing rough surface for ingrowth of fibrous tissue, preferably about a peripheral boundary. The component can be made of metal, and have the rough surface provided by porous metal coating. When the prosthesis is implanted, the extramedullary rough surface engenders ingrowth of soft fibrous tissue so that it forms, as it were, a reconstituted capsular “bag” in which wear debris from the joint, for example, ultra high molecular weight polyethylene wear debris, is trapped, thus keeping those particles from gaining access to supporting bone at the bone-prosthetic interface. And so, with mitigation of wear debris dispersion, debris wear-induced osteolysis can be ameliorated.

Abstract: Arthroplasty devices having improved bone in growth to provide a more secure connection within the body. Different embodiments disclosed include devices having threaded intramedullary components, devices configured to receive bone growth promoting substances, devices with resorbable components, and devices configured to reduce shear stress.

Abstract: An Apparatus for the preparation of a femur bone for the cement-free implantation of a prosthesis having a so-called press-fit-effect, the prosthesis having a distal part (2, 2A) corresponding to a diaphysial region of the femur (1, 1A), a proximal part (3, 3A) corresponding to a metaphysial region of the femur and an intermediate region (4, 4A) in which the press-fit-effect is preferably provided and which corresponds to a metaphysial-diaphysial region, with the height of the prosthesis being variable depending on the morpho-type and degree of bone damage is described which is characterized in that the apparatus consists of a modulatable rasp (10) including a plurality of parts, at least one of which has a conical distal part (10A) of a single size and of a single shape, there being at least first and second proximal parts (10B) of substantially different basic shapes, each of said first and second proximal parts being provided in a plurality of increasing heights (H), there being releasable connection means

Abstract: A series of humeral stems, each stem including an axial bore and longitudinal slots along the distal end to allow for distal compression. The compression force necessary to compress the distal diameter of each stem varies by stem diameter. Thus, as the stem diameter increases through the series, the compression force decreases. The axial bore and longitudinal slots together form a series of stem segments that assume the shape of the medullary canal, reducing the force exerted upon the canal by the humeral stem.

Abstract: Arthroplasty devices having improved bone in growth to provide a more secure connection within the body. Different embodiments disclosed include devices having threaded intramedullary components, devices configured to receive bone growth promoting substances, devices with resorbable components, and devices configured to reduce shear stress.

Abstract: The invention relates to a hollow rasp for preparing a tubular bone in which a post-shaped endoprosthesis is inserted. A manipulating instrument can be proximally coupled to the rasp. The rasp comprises a metal grid network and a plurality of metal rasp elements. The metal rasp elements are studded at least at junctions of the metal grid network and are an integral part of a material forming the grid network.

Abstract: A hollow endoprosthesis including a metal grid network, metal particles mounted at least at junctions of the metal grid network, and a solid metal portion. Each of the metal particles includes a basic body and at least three pins projecting radially from the basic body, and is an integral part of a material forming the grid network.

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.