Abstract: A method of inserting a spinal stabilization system into a patient generally comprises inserting a first positioning tool through a first location on a patient's skin and along a path generally toward a first vertebral anchor, coupling an end of the first positioning tool to the first vertebral anchor, positioning at least a portion of a delivery device over a connecting element, and inserting the delivery device and the connecting element through the patient's skin at the first location and along at least a portion of the first positioning tool. The first positioning tool is configured to facilitate directing the delivery device and connecting element generally toward a second vertebral anchor within the patient's body.

Abstract: In some examples, an apparatus includes a working surface including at least one material removal member. The material removal member is configured to remove at least some of a first portion of a first material. A protrusion extends outwardly from the working surface. The protrusion extends beyond the at least one material removal member by a first distance. The protrusion is configured to inhibit the at least one material removal member from removing at least a second portion of the first material. The second portion has a thickness substantially equal to the first distance.

Abstract: The present invention provides a spinous process implant and associated methods. In one aspect of the invention, the implant includes a spacer that is connectable to two extensions. One of the two extensions is connectable to the spacer at a first end and coupled to the spacer by a rotational connection. The other of the two extensions is movably connectable to the second end of the spacer and translatable over the outer surface of the spacer from the second end.

Abstract: The present disclosure provides an intramedullary nail assembly comprising an intramedullary nail and an insert sleeve. The intramedullary nail has a nail longitudinal axis and comprises a cavity being accessible from a nail proximal end, the cavity being confined by a nail inner wall, the cavity having a cavity longitudinal axis. The nail inner wall is provided with a predominantly longitudinal groove and a predominantly transverse groove, the transverse groove and the longitudinal groove communicating with each other at a junction. The insert sleeve is configured to be received within the cavity and comprises a cam radially protruding from the insert sleeve and sized to mate with each of the longitudinal and transverse grooves such that the cam is displaceable within the longitudinal groove from a longitudinal groove proximal end to the junction and is further displaceable towards a terminal end of the transverse groove.

Abstract: An orthopedic prosthesis and a method for rapidly manufacturing the same are provided. The orthopedic prosthesis includes a solid bearing layer, a porous bone-ingrowth layer, and an interdigitating layer therebetween. A laser sintering technique is performed to manufacture the orthopedic prosthesis.

Abstract: A prosthetic inserter includes an inserter head having at least first and second bosses, at least one of the bosses movable from a first position to a second position, that couple the inserter to a femoral provisional component via a pair of corresponding apertures, such as drill holes, within the articulating surfaces of a selected one of a series of femoral provisional components. Each provisional component of the series is capable of having different aperture distances measured between a respective pair of apertures. The bosses of the inserter are biased into an engagement position in which the inserter can be secured to a femoral provisional component to eliminate the need for an external engagement force to be supplied to the inserter.

Abstract: A system and associated instruments for locating, and accurately and controllably delivering, a device to an area sufficiently near a bone defect using anatomical landmarks is provided. The instruments allow the surgeon to navigate to the area around the bone defect quickly and easily, while so facilitating proper insertion of the device. In some embodiments, the defect is located on a femur. Guide instruments having a plurality of device portals are also provided for use as standalone instruments or as accessories to the system. In addition, a protective guide sleeve is provided for the insert of small diameter devices.

Abstract: The present invention provides a spinal implant for placement between adjacent processes of the human spine. In some embodiments the spinal implant includes a spacer and one or more retention members. In some embodiments, the retention members are fixed relative to the spacer and in other embodiments the retention members are deployable from a first or compact or stowed position to a second or expanded or deployed position. In some embodiments the spacer is expandable from a first size to a second size. In some embodiments the spacer has a tapered body.

Abstract: An implant system for total shoulder arthroplasties, hemi shoulder arthroplasties, and “reverse” total shoulder arthroplasties including a humeral stem having an enlarged head portion with interfaces adapted to removably receive various modular interchangeable components, such as articulating liners, spacers, and adapter inserts. The humeral stem functions as a universal platform that may be used in either conventional or “reverse” total shoulder arthroplasties, as well as hemi shoulder arthroplasties, and may remain implanted in place during a revision in which the implant system is converted between the foregoing configurations, for example.

Abstract: A vertebral column correction system for correcting a spinal deformity without fusing the joint segments is disclosed. The vertebral column correction system may have first and second vertebral anchors secured to first and second vertebrae. The vertebral column correction system may further comprise one or more intermediate vertebral anchors secured to vertebrae between the first and second vertebrae. A connection member may be disposed within a head portion of the vertebral anchors. At least a portion of the connection member may be a flexible member, such as a flexible cord, configured for tensioning between at least two vertebral anchors for providing a desired amount of tension to apply a correctional force to the spinal column. A spring member, or other tensioning member, may maintain the tension of the connection member.

Abstract: An angled instrument assembly includes an angled sleeve, a driver shaft, and a tool bit. The angled sleeve includes a straight passage segment that meets an angled passage segment at a junction. The junction includes an inner elbow and an outer elbow. Material is removed from the inner surface of the inner elbow in order to improve the ease with which the driver shaft can be moved in and out of the angled sleeve. The assembly can also include drafted female or male engagement bodies for facilitating the engagement and disengagement of the tool bit with a tool bit engagement assembly located at the distal end of the driver shaft.

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.

Abstract: Embodiments provide methods, apparatuses, and systems for fixation of a fractured bone. In various embodiments, the systems and plates may provide elastic suspension of the receiving holes relative to the osteosynthesis plate. This elastic suspension may promote load distribution between the screws that connect a bone segment to the plate, thereby reducing stress risers and load shielding effect. In addition, stress at the screw holes, and within the construct as a whole, is reduced by incorporation of these elastic elements in the plate. Additionally, in some embodiments, for instance if fracture healing by callus formation is desired, elastic suspension of the receiving holes relative to the osteosynthesis plate may enable small, controlled amounts of relative motion between bone fragments connected by the plate, which may promote fracture healing by callus formation.

Abstract: The present disclosure includes a method for reducing a bone fracture and an apparatus such as a cable button for use with a bone plate, the cable button including cable button threads, a plurality of cable button apertures, a hex socket, and a hex opening. The present disclosure also includes a method for reducing a bone fracture and an apparatus such as a cable button for use with a bone plate, the cable button including a plurality of legs, where a leg includes a protrusion, where the protrusion engages the bone plate, and the cable button defines at least one cable button aperture.

Abstract: An orthopedic tibial prosthesis includes a tibial baseplate sized and shaped to cover substantially all of a resected proximal tibial surface, and a tibial bearing component sized to leave a posteromedial portion of the tibial baseplate exposed when the tibial bearing component is mounted to the baseplate. The exposed posteromedial portion of the tibial baseplate includes a chamfered profile which cooperates with a correspondingly chamfered profile at a posteromedial edge of the tibial bearing component to create a substantially continuous chamfer extending from the resected tibial surface to the medial articular surface of the tibial bearing component. Advantageously, this chamfer leaves an absence of material (i.e., a relief or void) at the posteromedial edge of the tibial prosthesis, thereby enabling deep flexion of the prosthesis without impingement between the tibial prosthesis and adjacent anatomic tissues or prosthetic structures.

Abstract: A tibial prosthesis can include a bearing component and a tibial tray. The bearing component can include at least one concave articulating surface, a distal surface opposite said concave articulating surface, and a notch formed in said distal surface. The notch can define a longitudinal axis, the longitudinal axis defining an offset axis angle relative to the sagittal plane. The offset axis angle can range from greater than zero degrees to about 90 degrees. The tibial tray can include a support surface capable of supporting said bearing component, the support surface having a lateral edge and a medial edge opposite said lateral edge. The tibial tray can further include a boss having a longitudinal axis, the longitudinal axis angled with respect to the sagittal plane. The boss can be lockingly engageable with said notch along said offset axis angle to lock said tibial tray to said bearing component.

Abstract: An orthopedic tibial prosthesis includes a tibial baseplate with features designed for use with small-stature knee-replacement patients. The tibial prosthesis may include a shortened tibial keel, tibial keel fins which define a large angle with respect to a longitudinal axis of the keel, and/or tibial keel fins which extend along less than the entire longitudinal extent of the keel.

Abstract: The present disclosure relates to a shoulder prosthesis comprising a glenoidal component having a glenoidal articulation surface and a humeral component having a humeral articulation surface, and a separate mobile glenohumeral bearing component comprising a glenoidal bearing surface and a humeral bearing surface arranged on opposite sides of the glenohumeral bearing component. The glenoidal bearing surface contacts in an implanted state the glenoidal articulation surface and/or the humeral bearing surface contacts in an implanted state the humeral articulation surface. At least one of the glenoidal and humeral bearing surfaces is concave. The glenohumeral bearing component is disposed in an implanted state between the glenoidal component and the humeral component. Both the glenoidal and humeral articulation surfaces are convex.

Abstract: The present disclosure provides a provisional tibial prosthesis system for a set of prosthetic knee joints for implantation in a natural knee, the provisional tibial prosthesis system including a bearing component and a bearing support, the spacing of the bearing component from the bearing support is adjustable to allow for representation of a variety of different sized final tibial prostheses. In this system, only one provisional bearing component corresponding to each level of constraint is needed and shims are used to adjust the spacing of the bearing component from the bearing support. The shims are slidably insertable between the bearing component and the bearing support in an anterior/posterior direction to allow for adjustment of the spacing of the bearing component from the bearing support. The number of provisional components needed during knee surgery is reduced and adjustment of the system only requires the knee joint to be distracted by a distance equal to the height of a particular shim.

Abstract: The invention relates to a shaft for a femoral neck prosthesis, which comprises an anchoring area (27, 29) which is arranged inside the femur in order to anchor the prosthesis into bone, a head area which is axially adjacent to the anchoring area (27, 29) on the proximal side, said head area comprising a device (13) which is connected to the prosthesis head (15), in addition to a distal end which is arranged opposite the head area in the axial direction of the anchoring area (27, 29). The invention is characterised in that the maximum cross-sectional dimension of the head area is at the most equal and, in particular, smaller than the maximum diameter of the anchoring area (27, 29), in such a manner that the maximum cross-sectional dimension of the shaft (11) is in the anchoring area (27, 29).