Abstract: A prosthetic stem is configured to reduce the perioperative and intraoperative risk of catastrophic medical complications and death that may be caused by BCIS. The prosthetic stem includes one or more internal channels that are configured to self-regulate intramedullary pressure within a prepared bone channel as the stem is inserted into the channel, thus reducing the likelihood of BCIS without sacrificing biomechanics and maintaining a reliable and repeatable implantation process. The stem includes a head and a body, wherein the head is configured to serve as a joint replacement and the body is configured for insertion into the prepared bone channel of a patient. One or more internal channels in the stem are configured to control the pressure within the prepared bone channel during insertion of the stem into the channel, particularly by forming a path through which excess cement may flow as the stem proceeds into the prepared bone channel.

Abstract: Photodynamic devices for replacement of an articular head of a bone are provided. In an embodiment, a photodynamic device includes a photodynamic support member and an articular member attachable, either fixedly or removably, to the photodynamic support member and having a bearing surface. In an embodiment, the articular member includes a recess designed to receive the photodynamic support member. In an embodiment, the photodynamic support member includes an opening into which a shaft of the articular member can be inserted to attach the articular member to the photodynamic support member.

Abstract: An external intra-pelvic fundus vesicae support disposed at the outer fundus vesicae position and fixing the front end to the pelvic pecten pubis position to lift internal organs. An injection channel is provided inside an external intra-pelvic fundus vesicae support structure, and a screw hole is formed at an input hole, so that the support can be connected to an in-vitro device. According to the external intra-pelvic fundus vesicae support, a tomoscan three-dimensional modeling technology is used to generate a model file which completely conforms to physiological shapes of the pelvic pecten pubis and the outer fundus vesicae and the spatial form of the abdominal cavity of a typical person, and the external intra-pelvic fundus vesicae support of a frame structure and medical material quality is obtained using 3-D printing technologies. Before a surgery is conducted, a virtual reality technology is used to simulate and verify a surgical safety scheme.

Abstract: A bone graft delivery system includes an elongate tube configured to couple to the handle and receive a bone graft material and a rasp. The rasp includes a lumen configured to receive at least a portion of the elongate tube, a rasping surface configured to decorticate bone, one or more openings configured to deliver bone graft material from the elongate tube when the lumen receives at least a portion of the elongate tube, and a handle portion configured to be gripped in use to facilitate movement of the rasping surface to decorticate bone.

Abstract: Photodynamic devices for replacement of an articular head of a bone are provided. In an embodiment, a photodynamic device includes a photodynamic support member and an articular member attachable, either fixedly or removably, to the photodynamic support member and having a bearing surface. In an embodiment, the articular member includes a recess designed to receive the photodynamic support member. In an embodiment, the photodynamic support member includes an opening into which a shaft of the articular member can be inserted to attach the articular member to the photodynamic support member.

Abstract: Systems, devices, and methods for providing orthopedic augments having recessed pockets that receive a fixation material. The orthopedic augments include an outer surface that interfaces with a patient's tissue or bone, and an inner surface that interfaces with an implant, the inner surface defining a recessed pocket configured to receive a fixation material, a rim around at least a portion of the recessed pocket, and a port in the rim, wherein the recessed pocket extends along the inner surface in at least a direction laterally from the port.

Abstract: Photodynamic devices for replacement of an articular head of a bone are provided. In an embodiment, a photodynamic device includes a photodynamic support member and an articular member attachable, either fixedly or removably, to the photodynamic support member and having a bearing surface. In an embodiment, the articular member includes a recess designed to receive the photodynamic support member. In an embodiment, the photodynamic support member includes an opening into which a shaft of the articular member can be inserted to attach the articular member to the photodynamic support member.

Abstract: A method of reinforcing a femoral neck comprises creating a bore proximate to at least one of a Ward's triangle and a greater trochanter, creating at least one cavity in a cancellous bone region of the femoral neck, inserting a substantially collapsed support structure through the bore and into the at least one cavity, expanding the support structure, and allowing at least a portion of the load from the femoral neck bone to be transferred to the support structure. The support structure compresses at least a portion of the cancellous bone upon expansion. A cavity created by the expansion is adapted to receive a filler material such as, but not limited to, bone cement.

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 includes an implant defining an attachment surface thereon. A porous insert is selectively coupled to the implant. The porous insert is adapted to be received at the attachment surface of the implant in a retained position. The porous insert is adapted to facilitate tissue ingrowth. In one embodiment the implant comprises a femoral component. The femoral component comprises an inner condylar portion having a first and second lateral sidewalls, an anterior wall and a posterior wall defining a box. The box defines the attachment surface. In other embodiments, the implant comprises a hip stem and an acetabular shell.

Abstract: An artificial cement-less hip prosthesis stem comprises an inner construct 7 which reacts with a load acting on a hip joint and an outer construct 8 for transmitting the load acting on the inner construct to a femur 1. The inner construct has an inner body 7B which reacts with the load transmitted from a neck 7A. The outer construct has both an outer body 8A which is bell mouth-shaped toward an epiphysis so as to surround the inner body 7B and a leg 8B extending toward a medullary cavity. The torsional rigidity given to the proximal end and the distal end of the outer body 8A and the leg 8B is regulated so as to be lower than the torsional rigidity given to an intermediate portion 18 of the outer body 8A.

Abstract: The present invention relates to a knee joint prosthesis including femoral and tibial components. The bodies of the components possess a network of channels which may be used to deliver bone cement to the component bone interface after the components are implanted. The body of the femoral component possesses a network of channels which is in communication with a bore on the distal surface of the component which may be used to deliver bone cement into the network of channels after the component is implanted. The body of the tibial component possesses a network of channels which is in communication with a bore on the proximal surface of the component which may be used to deliver bone cement into the network of channels after the component is implanted. The components are suitable for implantation using arthroscopic as well as open surgical procedures. The components may be used as unicondylar implants in either compartment of the knee or in both compartments of the knee.

Abstract: A temporary femoral implant system has a porous mold and a femoral component. The system fits at least partially in a femoral cavity. The mold has a wall with an interior surface and an exterior surface forming an interior space for receiving an antibiotic bone cement. The mold allows the antibiotic to diffuse through the wall to the exterior surface. The femoral component has a stem portion received within the mold. A method of using the implant system includes providing an implant system comprising a mold and a femoral component, inserting the mold into the femoral cavity with the exterior surface facing the femoral cavity, inserting the stem portion of a femoral component into the interior space of the mold and filling the interior space of the mold with an antibiotic bone cement.

Abstract: The present invention is directed to an inflatable device for use in restoring the anatomy of diseased or fractured bone. The inflatable device may be a balloon of varied size or shape to conform to the bone to be treated and may be deployed in any type of bone where collapsed fractures of cortical bone may be treated by restoring the bone from its inner surface. Once the bone has been sufficiently restored the balloons may be deflated and removed, or may remain inside the bone. The balloon may have multiple layers to provide desired surface characteristics, resistance to puncture and tearing, or other beneficial properties, as appropriate for the particular application of the device.

Abstract: The nucleus of an intervertebral disc is replaced with a construct including a distendable sack or balloon which, following insertion at a surgical site, is inflated with a hardenable material and is detached in situ when the injected material has hardened. Preferably, two nested balloons are inserted, and then are filled with materials which have different hardnesses when cured, to simulate a natural disc.

Abstract: Apparatus and methods are disposed for maintaining the proper positioning of a prosthetic implant having proximal and distal ends within a prepared bone cavity during cement injection and curing. First stabilization means, implantable within the bone cavity, minimize lateral movement of the distal end of the implant, while second stabilization means, physically separate from the means for minimizing lateral movement of the distal end of the implant, minimize both the lateral movement of the proximal end of the implant and the rotational movement of the implant overall. In the preferred embodiment, the second stabilization means includes an apertured cap removably securable to the end of a bone having the prepared cavity through which the implant is inserted and held in place.

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: A stem of an artificial hip joint is capable of removing a gap that may be formed between a proximal portion of a femur and a backside of the stem. The stem has an upper end portion to face a proximal side and a backside to face a greater trochanter and is adapted for insertion into, and fixation to, a medullary space of a femur. The stem has a through bore opened both to the upper end portion and the vicinity of proximal end of the backside.

Abstract: A bone prosthesis for implantation at a joint includes a stem having a tip generally at one end thereof. The stem is sized and shaped for reception in a bone at the joint such that the tip of the stem is exposed to locations outside of the bone. The stem has a passageway extending from a first location on the bone prosthesis to a second location on the bone prosthesis.

Abstract: An artificial joint is capable of harmoniously connecting the artificial joint, cement and a bone and facilitating effusion of the cement at the time of implantation, as well as diminishing the stress applied thereto. The artificial joint includes a head, a neck and a stem, the stem being coated in advance with cement so as to easily bond the cement to cement filled in a bone cavity of a human femur. An effusion path for effusing the cement filled in the bone cavity is formed in a longitudinal direction on a surface of the cement coated on the stem so that the cement filled in the bone cavity of the human femur can be easily effused upward through the effusion path when the stem is inserted.

Abstract: The present invention is directed to an inflatable device for use in restoring the anatomy of diseased or fractured bone. The inflatable device may be a balloon of varied size or shape to conform to the bone to be treated and may be deployed in any type of bone where collapsed fractures of cortical bone may be treated by restoring the bone from its inner surface. Once the bone has been sufficiently restored the balloons may be deflated and removed, or may remain inside the bone. The balloon may have multiple layers to provide desired surface characteristics, resistance to puncture and tearing, or other beneficial properties, as appropriate for the particular application of the device.

Abstract: A stem of an artificial hip joint is capable of removing a gap that may be formed between a proximal portion of a femur and a backside of the stem. The stem has an upper end portion 11 to face a proximal side and a backside 15 to face a greater trochanter 33 and is adapted for insertion into, and fixation to, a medullary space of a femur, and the stem has a through bore 17 opened both to said upper end portion and the vicinity of proximal end of said backside.

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.

Abstract: A cement jacket for a cemented artificial joint stem, the cement jacket including a main body with a hollow interior and an open upper end for receiving and enclosing at least a part of a stem of an artificial joint, the cement jacket being shaped and adapted for longitudinal insertion in an opening formed in a bone canal of a human body, the cement jacket being made of cement and reinforced by imbedded wire or fiber and having an inner surface coated with a plastic film having a high resistance to abrasion, and the outer surface of the cement jacket is formed with discharging paths in the longitudinal direction so that excessive cement paste previously poured into the bone canal for the surgical purpose can be easily discharged upward at the time of inserting the jacket.

Abstract: A prosthesis provided with a stem at least part of which is enclosed in a mantle and which is for insertion in a bone cavity and attachment thereto by cement, said mantle having a wall thickness which is increased towards its proximal end to provide an outwardly projecting proximal balcony and which is dimensioned and adapted to locate the stem in a predetermined position within the cross-sectional area of the bone cavity at or towards the proximal end thereof.

Abstract: A centralizer (1) is provided with a hollow body (2) and a plurality of equally spaced arms (4). The arms (4) extend in the form of cup handles from the hollow body (2). Each arm (4) has a variable cross-section along its length with the cross-section becoming increasingly ovoid towards one end of the arm (4).