Abstract: The present invention relates to a straight stem (10) for the implantation into a proximal femur, the stem (10) comprising a proximal stem section (12) and a distal stem section (14), the distal stem section (14) having a distal end (24) and a distal tip (26) arranged directly adjacent to the distal end (24) and defining a distalmost point of the distal end (24), the stem (10) having, in an anterior-posterior view, a medial contour and a lateral contour, and the stem (10) having a straight stem center axis (20) between the medial contour and the lateral contour, wherein the distal end (24), in an anterior-posterior view, has a convexly curved contour, and wherein the convexly curved contour of the distal end (24) merges with straight sections (46, 48) of the medial contour and of the lateral contour at a medial merging point (22) and a lateral merging point (28), respectively, wherein the medial merging point (22) and the lateral merging point (28) are offset with respect to each other in a direction parallel

Abstract: The present disclosure relates to an insert sleeve (19) designed for being inserted into a through hole (17) of an implant (11), comprising a body (21) with a through hole (23) defining an axial direction (29) for receiving a bone anchoring element (25), in particular a bone screw, said body (21) being made of a material having a first modulus of elasticity and including multiple recesses (27) arranged in circumferential direction around said through hole (23) of said insert sleeve (19) for reducing a stiffness of said insert sleeve (19) in a direction transverse (31, 33) to said axial direction (29). At least one of said recesses (27) is filled with a filler material (41) having a second modulus of elasticity different from said first modulus of elasticity.

Abstract: A femur fixation device including an elongated nail configured for insertion into the medullary canal of the femur and a buttress element extending from the elongated nail. The buttress element is configured to reinforce the lesser trochanter region of the femur and assist in stabilizing the head portion of the femur.

Abstract: The present disclosure relates to porous orthopedic implants made from polymer preforms and a method of manufacturing the same. A polymer material may be formed into a preform, such as by an injection molding process or an additive manufacturing process. In an exemplary embodiment, the overall shape and the porous framework of the preform is predetermined to be substantially the same as the overall shape and the porous framework of the final orthopedic implant. Then, the preform may be pyrolyzed and coated with metal to form the final orthopedic implant.

Abstract: A prosthetic femoral component (10) for an orthopaedic prosthesis has a canted patellar groove adapted for optimal patella/component interaction, with the component configured to have a medial or lateral cant depending upon the method of implantation. The femoral component defines a distal “component transverse plane,” which is a plane tangent to the distal-most points of the component condyles (12,14). In a “mechanical” implantation, the component transverse plane is substantially normal to the mechanical femoral axis of the femur after the component has been implanted. Where the femoral component is configured to be “mechanically oriented” in this manner, the component has a medially canted patellar groove. On the other hand, an “anatomic” implantation is one in which, after the component has been implanted, the component transverse plane is substantially parallel to an “anatomic” transverse plane.

Abstract: A spinal device and associated method are provided for spreading of first and second vertebral elements, each of the first and second vertebral elements having a circumferential surface defining a vertebral body and a pedicle having a pedicle root portion adjacent the circumferential surface. The device includes a first end member having at least one surface adapted to conform to at least one of the circumferential surface and the pedicle root portion of the first vertebral element, and a second end member having at least one surface adapted to conform to at least one of the circumferential surface and the pedicle root portion of the second vertebral element. The device further includes a resilient member extending between the first and second end members and being adapted to exert a force against the first and second vertebral elements.

Abstract: A subtalar implant (1) for stabilizing the subtalar joint in the human foot includes a longitudinal axis (L) extending between a front end (13) and a rear end (14), wherein a first anchor portion (2) is arranged to the side of the longitudinal axis (L) and a second anchor portion (3) is arranged to the side of the longitudinal axis (L). In accordance with the invention, a spreading mechanism (5) to spread apart the implant as a result of relative displacement of the first and second anchor portion (2, 3) at an angle to the longitudinal axis (L) are provided.

Abstract: A spinal device and associated method are provided for spreading of first and second vertebral elements, each of the first and second vertebral elements having a circumferential surface defining a vertebral body and a pedicle having a pedicle root portion adjacent the circumferential surface. The device includes a first end member having at least one surface adapted to conform to at least one of the circumferential surface and the pedicle root portion of the first vertebral element, and a second end member having at least one surface adapted to conform to at least one of the circumferential surface and the pedicle root portion of the second vertebral element. The device further includes a resilient member extending between the first and second end members and being adapted to exert a force against the first and second vertebral elements.

Abstract: A surgical mid-foot compression pin (1), includes a core region (2) having a drive, a front thread portion (6) having a front outer thread (7), a rear thread portion (9) having a rear outer thread (10), and a middle portion (8) arranged between the thread portions, the pitch of the front outer thread (S1) being greater than that of the rear outer thread (10) so as to achieve a compression. In accordance with the invention, the rear outer thread (10) has a conical sleeve contour, which tapers in the direction of the front end (3) of the compression pin (1).

Abstract: A dynamic stabilization system for stabilizing a vertebral segment of a spine. The system includes a first vertebral anchor, a second vertebral anchor and a cord. The system may also include a spacer positioned between the first and second vertebral anchor through which the cord extends. The first vertebral anchor is configured to be secured to a first vertebra and the second vertebral anchor is configured to be secured to a second vertebra. The cord is extendable from the first vertebral anchor to the second vertebral anchor. The cord has a variable stiffness through a range of displacement, wherein the stiffness of the cord increases as an applied tensile force on the cord is increased.

Abstract: The present disclosure relates to devices and methods for verifying compatibility between cooperating parts of a joint prosthesis. The compatibility between the cooperating parts is with respect to at least one articulation parameter.

Abstract: An implant is described for fracture treatment, comprising an elongate and in particular substantially rotationally symmetrical base body (20), in particular an implant shaft, and an anchoring section (10), wherein the anchorage section has an outer surface of a porous biocompatible material at least in part, and wherein the anchorage section is arranged in an axial end region of the implant and is releasably connectable to the base body.

Abstract: An orthopaedic knee joint prosthesis (10) provides guided motion in a wide range of motion, and in both extension and flexion. In flexion, a tibial bearing component (16) shifts to a first position in which a posterior cam (36) formed in a femoral component (12) engages a tibial spine (18) coupled to a tibial component (14). Contact between the posterior cam and the spine guides the motion profile of the knee joint prosthesis throughout a wide range of flexion movement. In extension, the bearing component shifts to a second position in which an anterior cam (34) formed in the femoral component engages the spine. Contact between the anterior cam and spine guides the motion profile of the knee joint prosthesis throughout a wide range of extension. The anterior and posterior cams, mobile bearing component, and tibial component-mounted spine cooperate to facilitate guided flexion and extension of the knee joint prosthesis throughout a wide range of motion.

Abstract: The present disclosure relates to a stemless shoulder prosthesis comprising a fixation device for fixing the prosthesis to a resected humerus bone, the fixation device comprising a base portion (11, 31, 32) and anchoring means (12, 12?), the base portion (11, 31, 32) having a distal side adapted to contact a resection plane of the bone and a proximal side for carrying a humeral head. The anchoring means (12, 12?) are connected to the distal side of the base portion (11, 31, 32) and adapted to fix the prosthesis to the bone. The anchoring means (12, 12?) define a central axis (C), wherein the anchoring means (12, 12?) comprise a plurality of protrusions (13, 13?, 13a, 13b, 13c) projecting from the base portion (11, 31, 32), each protrusion (13, 13?, 13a, 13b, 13c) extending between an inner end (I) and an outer end (O). The protrusions (13, 13?, 13a, 13b, 13c) define a free central space (F) around the central axis (C).

Abstract: The invention relates to an intervertebral disk implant having two implant plates contacting prepared vertebral body surfaces in the implanted state and an implant core which can be introduced between the implant plates. The invention further relates to a method for the manufacture of an intervertebral disk implant.

Abstract: An orthopedic assembly for stabilizing a fractured bone. The orthopedic assembly includes a support structure and an anchor. The anchor includes a first portion and a second portion moveably coupled to the first portion to adjust an angular orientation of the anchor relative to the femur.

Abstract: A method is disclosed for producing polymers with a neutral color tone, wherein a blue and red dye are added before entry into the last polyreaction stage, wherein adjustment of a neutral color tone of the polymer, using a total dye concentration in the polymer of no more than 3 ppm and a proportion of the blue dye in the resulting dye mixture of at least 50% by weight, occurs through independent adjustment of a and b color values in the Lab color space by determination of a and b color values of the polymer without addition of dyes, establishment of the total dye concentration depending on the b-value shift to be achieved, establishment of the required mixture ratio of the colors red and blue depending on the a-value shift to be achieved, and metering of the established content of dye mixture into the reaction mixture.

Abstract: In some examples, a method for at least one of preparation or machining of a femoral head formed on a neck of a femur includes selecting an instrument including probing forceps and a guide element including a centering axis. The guide element is coupled to the probing forceps at first and second coupling points disposed along the centering axis such that the centering axis is disposed in a central plane of the probing forceps independent of an opening angle of the probing forceps. The probing forceps are closed with probing jaws symmetrically contacting the neck of the femur at opposite sides with respect to an axis of the neck of the femur. The guide element self-adjusts with closing of the probing forceps so that the centering axis is automatically aligned in the middle with respect to the two oppositely disposed sides of the neck of the femur.

Abstract: Rasps for preparing bones of various patients to receive a prosthetic implant and a method for using the same. Multiple rasps may be provided as a set. Within the set, the rasps generally correspond to the size and shape of a single prosthetic implant, such as a prosthetic femoral hip stem, and have a range of bone removal and bone compression capabilities to account for unique bone characteristics of the various patients. A surgeon may select a desired rasp from the set provided depending on the patient's unique bone characteristics.