Abstract: The present disclosure relates to a rotor assembly for a peristaltic pump. The pump includes a first rotor having a plurality of rollers and a second rotor, coupled to the first rotor, having a plurality of rollers. The rollers of the first and second rotors are located at an angle of about 45° relative to each other. In an embodiment, the first rotor and the second rotor are circular. In another embodiment, the rollers of the first rotor are equally spaced or located at an angle, about 90°, relative to each other. In yet another embodiment, the rollers of the second rotor are equally spaced or located at an angle, about 90°, relative to each other. A peristaltic pump and a method of supplying fluid to a surgical area are also disclosed.

Abstract: Embodiments of the present invention provide patellar component designs that are optimally shaped to help reduce shear force and accommodate slight implantation error. Further, they help lessen anterior knee pain, particularly during deep-flexion activities and help ease the transition during the range of knee movement in a controlled way.

Abstract: A multi-layer, fiber-reinforced composite orthopaedic fixation device having a design selected based on a desired characteristic of the orthopaedic fixation device. The design may be selected according to a model of the device, the model defining design constraints, and the design may comprise a pattern of the fiber angle for each layer. The selection of a design may be analyzed using finite element analysis to determine whether the design will comprise the desired characteristic.

Abstract: Oxidation resistant crosslinked ultrahigh molecular weight polyethylene (UHMWPE) is described, wherein at least two different additives in the manufacture synergistically increase the oxidation resistance of crosslinked UHMWPE. This allows the manufacture of oxidation resistant crosslinked UHMWPE using lower levels of additives and/or lower levels of crosslinking irradiation or chemicals. The lower levels of additives and/or crosslinking produce crosslinked UHMWPE having desired physical properties not possible without the synergistic interaction of the additives. This crosslinked UHMWPE may be used in medical prostheses such as in bearing components having desired physical properties such as wear resistance and oxidation resistance not possible without the synergistic interaction of the additives.

Abstract: An orthopaedic implant including a base portion and first and second transverse portions extending transversely from the base portion to thereby define an inner region of the implant sized for receipt of an end portion of a bone therein. The implant further includes at least one anchor structure projecting from the base portion and sized and configured for receipt within an opening formed in the end portion of the bone. The anchor structure extends along a longitudinal axis and includes a proximal end attached to the base portion and an opposite distal end, and further includes a tapered outer surface that inwardly tapers in a proximal-to-distal direction along the longitudinal axis. In one embodiment, the anchor structure also includes one or more grooves extending into the tapered outer surface, with a flowable material positioned about at least a portion of the tapered outer surface and positioned within the grooves, and with the flowable material configured to cure to a hardened state.

Abstract: There is provided a surgical saw blade for use in orthopaedic surgery. The saw blade comprising: a mounting cavity having a first substantially triangular-shaped opening and a second substantially triangular-shaped opening in communication with, and inverted relative to, the first opening, the first and second opening collectively define two mounting slots that form an angle relative to one another. In some embodiments, the planar portion further comprises an offset planar shelf. The offset shelf may be oriented along the length of the planar portion to allow for longitudinal reciprocation or may be oriented across the width of the planar portion to allow for lateral reciprocation.

Abstract: There is provided a tibial component comprising: a tibial tray with an inferior side; and a support member connected to the inferior side of the tibial tray, the support member having a stem portion, the support member further comprising at least one opening. In one embodiment, the at least one opening is constructed and arranged to receive a sawblade or an osteotome. In another embodiment, the at least one opening is comprised of solid material but is radio-lucent. In yet another embodiment, the at least one opening is comprised of solid material and is frangible.

Abstract: A system for targeting landmarks on devices such as surgical implants is disclosed. The system can include a field generator for generating one or more magnetic fields, an orthopaedic implant located within the magnetic fields, the implant having at least one landmark, a removable probe with a first magnetic sensor, a landmark identifier and a processor. The landmark identifier can contain a second sensor, or, alternatively, the field generator. The processor can utilize sensor data and, if desirable, field generator and other information, to generate and display the position and orientation of the sensor(s) in preferably six degrees of freedom, and thereby, to generate and display the position and orientation of the landmark(s). The system allows for blind targeting of one or more landmarks. The landmark identifier, field generator and/or drill motor may be disposed in an autoclavable housing.

Abstract: A method for performing shoulder arthroplasty or hemiarthroplasty is provided. The method includes generating navigational reference information relating to position and orientation of a body part forming at least a portion of the shoulder joint. The reference information may be stored in a computer. Navigational references are attached to the body part and an object. Information is received regarding the position and orientation of the object with respect to the body part and the object is navigated according to this information. The body part may be modified using the object and the modification may be displayed on a monitor associated with the computer. The navigational references may be used to track a shoulder arthroplasty trial component. Information is received regarding the position and orientation of the trial component with respect to the body part. This information is used to navigate the trial component to the body part.

Abstract: A receptacle for receiving a mating member in an orthopaedic joint, wherein the receptacle comprises: a first portion shaped so as to contact with the mating member, in normal use; a second portion shaped so as to not contact with the mating member, in normal use, wherein the first portion comprises a non-spherical surface. A mating member for being received by a receptacle, wherein the mating member comprises: a first portion shaped so as to contact with the receptacle, in normal use; a second portion shaped so as to not contact with the receptacle, in normal use, wherein the first portion comprises a non-spherical surface. Also disclosed are receptacles and heads of generally elliptical shape.

Abstract: A system for fixation of bone, including a bone plate with an opening comprising threads made of a first material and a fastener with a head at least partially comprising a polymeric material that is softer than the first material. In some embodiments, when the fastener is inserted into the first opening, the threads of the first opening form threads in the polymeric material on the head of the fastener and secure the fastener in place at one of a plurality of possible angles within the first opening. The first opening additionally accepts a fastener with a substantially spherical head for compression of a fracture, or a fastener with a threaded head that engages with the threads of the threaded opening. In some embodiments the first opening includes a substantially frustoconical-shaped top portion. In other embodiments there may be a second opening that is either non-threaded or comprises a plurality of protruding fins.

Abstract: Systems, devices and methods are disclosed for treating fractures. The systems, devices and methods may include one or both of an implant, such as an intramedullary nail, and a fastening assembly, such as a lag screw and compression screw assembly. The implant in some embodiments has a proximal section with a transverse aperture and a cross-section that may be shaped to more accurately conform to the anatomical shape of cortical bone and to provide additional strength and robustness in its lateral portions, preferably without requiring significant additional material. The fastening assembly may be received to slide, in a controlled way, in the transverse aperture of the implant. In some embodiments, the engaging member and the compression device are configured so that the compression device interacts with a portion of the implant and a portion of the engaging member to enable controlled movement between the first and second bone fragments.

Abstract: Methods, systems and devices for preventing prosthetic articulating surfaces from separating from each other. A containment system according to one embodiment seeks to prevent an implant stem head from dislocating from a prosthetic component while providing an increased range of motion over conventional constrained components. In one embodiment, an implant structural member includes a cavity and an opening having a lip, including a web along a portion of the lip. An implant stem head has a cooperating surface that corresponds with the web, so that when the cooperating surface of the implant stem head is aligned with the web, the head may be inserted into the implant structural member. The implant stem head is then rotated and the femoral stem component attached, thereby preventing dislocation of the head.

Abstract: A pin alignment guide may be placed on an end of a bone for guiding a pin along a central axis of the bone. The bone has a length extending away from the end of the bone. A body may be configured to overlie the end of the bone. The body may have a contact surface configured to contact the bone and a guide surface configured to guide a pin into the bone. A rod portion may be configured to extend along the length of the bone away from the end of the bone. An extension may be configured to attach to the body and extend away from the body, the extension further configured to couple to the rod portion, such that the rod portion may be aligned along the length of the bone thereby positioning the guide surface of the body to guide the pin.

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 a base 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: 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. Any of the implantable components may be include one or more porous surfaces. The porous surface may be textured by protrusions that connect to and extend from the surface. The sizes and concentration of the protrusions may be varied for specific applications to accommodate different implants and patient anatomies. A porous implant may also include one or more internal or external solid portions that strengthen the implant.

Abstract: A pre-assembled orthopaedic implant adapted for improved gas sterilization. The implant includes a first component adapted for assembly with a second component such that a mating surface of the first component is in close proximity with a mating surface of the second component. At least one gas conduit associated with the mating surface of the first component facilitates a sterilizing gas to penetrate into and dissipate from the interface defined by the mating surfaces.

Abstract: An apparatus for tissue repair includes first and second fixation members configured to secure tissue together, a flexible coupling member coupling the first and second fixation members, the flexible coupling member having two terminal ends, one of the two terminal ends terminating adjacent one of the first and second fixation members, the flexible coupling member slidably coupled to at least one of the first and second fixation members such that when the other of the two terminal ends of the flexible coupling member is pulled, a length of the flexible coupling member between the first and second fixation members is shortened, and a closed loop of flexible material, the flexible coupling member being slidably received through the closed loop of flexible material.

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 component may be expandable to allow for adjustment and custom fitting during implantation. An expandable implant may have a first portion and a second portion separated by a slit. An expansion member can be disposed between the first and second portions and can be actuated to displace the two portions relative to each other, increasing the size of the implant. Any number of slits and expandable sections can be included in the implant to provided more flexibility in the expansion of the implant.

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 augment provided for an acetabular implant may be adjustably positionable around the implant. An implant may have one or more slots that mate with connections on the augment and allow the augment to move within the slot. An augment may be translated, rotated, or moved in any other way to achieve a desired orientation prior to locking the augment in place relative to the implant. The augment may be locked by a screw or other locking mechanism that holds the augment in place. The locking mechanism may be releasable to allow for repositioning of the augment.