Abstract: Modular humeral implants and methods of use. A humeral implant can include a stem portion, a metaphyseal portion, a locking element, and an intermediate portion. The intermediate portion can include at least one spacer. Each spacer can include a proximal engagement feature, a distal engagement feature, a lumen extending longitudinally through the spacer, and a pin slidable within the lumen of the spacer. Distal movement of a locking element in the metaphyseal portion can translate the pin of each spacer to secure the metaphyseal portion, the intermediate portion, and the stem portion in a locked configuration.

Abstract: An orthopedic driver is provided that includes an elongate tubular body and an indicator assembly. The indicator assembly has a housing that has at least one opening and a visual indicator disposed in the at least one opening. The visual indicator is configured to be coupled with a guide pin such that lateral movement of the elongate tubular body relative to the guide pin causes the visual indicator to move between a flush or recessed configuration within the housing and an extended configuration. In the extended configuration, the visual indicator extends outward of an outer surface of the housing. The flush or recessed configuration corresponds to alignment of the guide pin relative to the elongate tubular body and the extended configuration corresponds to misalignment of the guide pin relative to the elongate tubular body.

Abstract: A glenoid component for coupling to a scapula of a subject includes a body. The body includes an articulation surface adapted to articulate with a humeral component, and the body further includes a distal surface adapted to face the glenoid of the scapula. The distal surface includes a base surface portion adapted to face a first portion of the glenoid. The distal surface further includes an augmented surface portion adapted to face a second portion of the glenoid. The base surface portion and the augmented surface portion define an obtuse angle therebetween.

Abstract: Described herein is a suture for connecting a human or animal tissue comprising a suture strand, wherein at least two protrusions are provided on the suture strand, the protrusions are provided spaced apart from each other along the suture strand. Also described herein is a soft anchor, the soft anchor having a proximal end and a distal end in an insertion direction. At the proximal end and the distal end the soft anchor includes respectively at least one opening for a suture. The proximal end and the distal end of the soft anchor are connected with at least one, in particular two, connecting portions. The soft anchor has a first state, in which it is adapted to be inserted into a bore in the insertion direction, and a second state, in which it is locked in a bore. In the first state, the distal end and the proximal end defines the extension of the soft anchor in insertion direction.

Abstract: A bone anchor inserter according to embodiments of the present invention includes a shaft configured to interface with a bone anchor, a proper depth indicator on the shaft, an upper visual indicator on the shaft, the upper visual indicator located adjacent to the proper depth indicator on a first side of the proper depth indicator furthest from the bone anchor, and a lower visual indicator on the shaft, the lower visual indicator located adjacent to the proper depth indicator on a second side of the proper depth indicator opposite from the first side, the lower visual indicator being visually distinct from the upper visual indicator.

Abstract: Reversed glenoid implants, and related kits and methods, are described that include an anchor member having a proximal head and a baseplate having a distal end with a first aperture sized to accept the proximal head of the anchor member. The proximal head is inserted along an un-threaded length thereof from the distal end into the first aperture, and the anchor member is restrained against axial translation with respect to the baseplate but is permitted to rotate with respect to the baseplate.

Abstract: A method and apparatus of reattaching a bone fragment to a proximal humerus of a humerus in a shoulder joint. The method includes introducing a distal end of the humeral nail into a medullary canal of the humerus. A first proximal screw is engaged with the bone fragment and a first proximal bore in the proximal end of the humeral nail to move the bone fragment toward the proximal humerus. The humeral nail and the attached bone fragment are rotated relative to the medullary canal of the humerus to position the bone fragment to an anatomically optimal location. The bone fragment is preferably one of a greater or lesser tuberosity of the proximal humerus. The method and apparatus can be used to reattach bone fragments in a variety of other joints.

Abstract: Modular humeral implants and methods of use. A humeral implant can include a stem portion, a metaphyseal portion, a locking element, and an intermediate portion. The intermediate portion can include at least one spacer. Each spacer can include a proximal engagement feature, a distal engagement feature, a lumen extending longitudinally through the spacer, and a pin slidable within the lumen of the spacer. Distal movement of a locking element in the metaphyseal portion can translate the pin of each spacer to secure the metaphyseal portion, the intermediate portion, and the stem portion in a locked configuration.

Abstract: A prosthesis that mechanically couples with both cancellous bone and cortical bone of a glenoid includes a head portion comprising a rear surface and an articular surface, an anchor member, and a plurality of deformable fins extending radially outward from the anchor member. The anchor member includes a distal end and a proximal end connected to the rear surface of the head portion. The plurality of deformable fins extend radially outward from the anchor member and includes at least a first proximal fin adjacent to the rear surface of the head portion positioned to engage with the cortical bone. The anchor member may also include at least one distal fin located proximate the distal end of the anchor member positioned to engage with the cancellous bone.

Abstract: Systems, apparatuses and methods for securing tissue to bone using a bone anchoring system are described. Methods and apparatuses may allow transformation between locked and unlocked states, thereby allowing adjustment of the tension in the suture. The apparatus and/or methods may allow unidirectional movement of a suture, while preventing slippage or movement of the suture and tissue in the opposite direction. Ends of a suture may be individually tensioned to adjust positioning of a tissue with respect to a bone.

Abstract: A glenoid component is provided to reduce glenoid loosening when implanted in orthopedic joint replacement/reconstruction, such for a shoulder. The glenoid component can include pegs or a keel and articulating surface geometry that uses complex, non-spherical geometry to recreate a level of constraint that is adequate, but not excessive, to thereby mitigate loosening of the glenoid component after implantation. In addition, some embodiments provide that peak stresses both within cement and at an interface of the cement and a supportive component can be reduced. Further, geometry of the pegs can allow stresses to be evenly applied to a cement mantle formed in the supportive component. Finally, the pegs can be configured to desired lengths in order to avoid placement in areas of the supportive component, for example, that have insufficient bone stock.

Abstract: Some embodiments of the present invention include a suture anchor with both knotless and knotted suture attachment capabilities, as well as methods for loading the suture in knotless and knotted configurations. Some embodiments of the present invention include a suture anchor with an inner implant body with a spreader that slides in relation to an outer expandable collar, such that pushing the expandable collar distally with an inserter causes the spreader to expand the collar against the surrounding bone to secure the suture anchor in place. Such embodiments may also include a detachment or breakaway feature between the inserter and the suture anchor to permit separation after anchor deployment. Some embodiments of the present invention include methods for deploying such suture anchors and expanding the expandable collars and/or detaching the inserter tools. Embodiments of the present invention may be used in various orthopedic applications such as, for example, shoulder repair.

Abstract: An orthopedic device and method of use are provided that incorporate complex, non-spherical articulating surfaces to allow a greater available range of motion compared with existing artificial shoulder joint and artificial hip joints. According to some embodiments, complex, non-spherical articulating surfaces can be incorporated on a humeral head and/or glenoid of a shoulder prosthesis. In other embodiments, complex, non-spherical articulating surfaces can be incorporated on the acetabulum and/or femoral head of a hip prosthesis. These non-spherical surfaces can be used to adjust constraint, joint thickness, soft tissue tension, moment and arc of motion, and in doing so, influence motion.

Abstract: The device (1) comprises a first snare (10) and a second snare (20), each of these snares comprising a contractable hollow elongated body (11, 21) which defines a longitudinal central axis (X10, X20) and which reduces its cross section when two opposed first (12, 22) and second (13, 23) ends thereof are axially moved away from each other. The first end (12) of the first snare (10) and the first end (22) of the second snare (20) are each open and adapted to be fitted and tightened around, respectively, two stumps (T1, T2) of a soft tissue (T) to be repaired. The second end (13) of the first snare (10) and the second end (23) of the second snare (20) are adapted to the axially pulled so that the second end of each of the two snares is passed alongside or through the body (11, 21) of the other snare.

Abstract: A set includes glenoid components that each include a body defining, on two of its opposite faces, respectively, a joint surface, intended to cooperate with a humeral head, and a bearing surface bearing against the socket of a shoulder blade. In this set, the glenoid components are provided in several different sizes, respectively defined by the dimensions of the joint surface of their body. At least two glenoid components of which the bearing surfaces respectively have different dimensional geometrics are provided so as to allow the surgeon to improve the durability of the mechanical cooperation between the implanted component and the operated socket.

Abstract: A surgical tool, enabling extraction of a prosthesis from a bony implantation site of that prosthesis, defines a proximo-distal axis and includes a distal end head adapted both to cut at least partially the bonding interface between the prosthesis and the bony material of the implantation site and to fix itself to the prosthesis by rotation centered on the proximo-distal axis, according to embodiments of the present invention.

Abstract: A suture anchor according to embodiments of the invention includes a body (102) having a proximal (121) and distal (125) ends and at least two suture paths open towards the proximal end and not open (e.g. looped around) towards the distal end and which are respectively capable of receiving a suture, and a proximal cavity (103) opening into a transverse cavity (104). The anchor may also include a transverse wall (105) arranged at least partially in the transverse cavity (104), and for each suture path, a distinct eyelet (112) for the passage of a suture through the transverse wall (105), so that a suture thread (162) in place in the anchor (100) forms a U with a first strand (162a) along the longitudinal axis (X-X), a second strand (162c) substantially parallel thereto, and an arc (162b) formed in the eyelet (112) and connecting the first and second strands.

Abstract: Systems, apparatuses and methods for securing tissue to bone using a bone anchoring system are described. Methods and apparatuses may allow transformation between locked and unlocked states, thereby allowing adjustment of the tension in the suture. The apparatus and/or methods may allow unidirectional movement of a suture, while preventing slippage or movement of the suture and tissue in the opposite direction. Ends of a suture may be individually tensioned to adjust positioning of a tissue with respect to a bone.