Abstract: An implant for fixation of a bone includes a shaft having a proximal end and a distal end, and a longitudinal axis defined between the proximal end and the distal end. A plurality of blades are disposed on the shaft, and are helically twisted about the longitudinal axis. At least one of the blades has a variable blade width that increases in a direction along the longitudinal axis. A mechanism for coupling the implant to a second fracture fixation implant may be provided separately or in combination.

Abstract: A bone cement comprising an acrylic polymer mixture which is formulated to have a relatively high viscosity for a relatively long window, due to distributions of molecular weights and/or sizes of acrylic beads.

Abstract: The present invention generally provides a polyaxial fixation device having a shank with a spherical head formed on a proximal end thereof, and a receiver member having an axial passage formed therein that is adapted to polyaxially seat the spherical head of the shank. The polyaxial bone screw further includes an engagement member that is adapted to provide sufficient friction between the spherical head and the receiver member to enable the shank to be maintained in a desired angular orientation before locking the spherical head within the receiver member.

Abstract: A system for locking an intramedullary nail to a bone includes a first plate sized and shaped to be inserted through a channel of an intramedullary nail and dimensioned to prevent its passing through a locking hole of the intramedullary nail and a second plate sized and shaped to be positioned along a portion of an exterior of a hole drilled in the bone and dimensioned to prevent its passing through the hole drilled in the bone along with a connector couplable to the first and second plates and slidable through the channel of the intramedullary nail to extend through the locking hole from an interior of the channel to an exterior of a bone in which the intramedullary nail has been inserted.

Abstract: A braid implant delivery and retraction device having a catheter, an expandable element and a delivery wire with distal, pusher, and recapture bumps. The expandable element having compressed, partially delivered, and implanted configurations. Delivering the braid can include engaging the distal bump till the braid is in the partially delivered configuration. If the user needs to recapture the braid, the recapture bump engages the braid proximally. To fully implant the braid, the distal bump is used until the braid is partially delivered and the distal bump disengages, now the pusher bump completes implanting by proximally pushing the braid completely out of the catheter.

Abstract: A device for containing a graft material includes an outer member formed via an outer mesh sheet biased toward a coiled configuration in which the outer mesh sheet is coiled about a longitudinal axis thereof so that, when the outer member is positioned about separated portions of a target bone in an operative position, the outer member reverts to the coiled configuration and contracts about and engages the separated portions. The device also includes an inner member formed via an inner mesh sheet coiled about a longitudinal axis thereof. The inner member is movable between a first biased coiled configuration and a second coiled configuration. A diameter of the inner member in the first coiled configuration is larger than a diameter of the inner member in the second coiled configuration.

Abstract: Methods for treating a patient having a disease or condition related to IVD degeneration are provided. The methods comprise administering cells obtained from human umbilical cord tissue, or administering pharmaceutical compositions comprising such cells or prepared from such cells. In some embodiments, administering the cells promotes repair and regeneration of degenerated IVD tissue in the patient. Pharmaceutical compositions for use in the inventive methods, as well as kits for practicing the methods are also provided.

Abstract: A modular femoral prosthesis system for an orthopedic hip implant and method of use is disclosed. The prosthesis system includes a femoral stem component and a plurality of collar components configured to be selectively coupled to the stem component in a fixed position adjacent to a neck of the stem component. Each of the collar components includes a base and is configured to secure an assembled femoral prosthesis to a patient's surgically prepared femur to provide stability for the assembled femoral prosthesis.

Abstract: A method of irradiating spinal tissue with red/NIR light, comprising: inserting a cannulated device defining a bore into the spinal column, wherein the bore contains an optically transparent substrate adapted to emit red/NIR light, and transmitting NIR/red light through the substrate to irradiate tissue within the spinal column.

Abstract: The disclosure extends to methods, systems, and computer program products for detecting whether an illumination source of an endoscope is in use (inside the body of a patient) versus not in use (outside the body of a patient). The disclosure relies on the fact that the working environment is lit solely by the endoscope and its components. Thus, communication between the illumination or light source controller and the imaging device, such as a surgical camera, is required. When the illumination or light source is turned off and the endoscope is outside the body, a sensor will detect ambient light alerting the illumination source controller that it is outside the body, which then keeps the illumination source off or at a low intensity level. Conversely, when the illumination source is turned off and the endoscope is inside the body, the sensor will not detect any light (or will detect only a very low level of light).

Abstract: An intramedullary device includes an intramedullary nail extending along a longitudinal axis from a proximal end to a distal end, the nail including a channel extending longitudinally therethrough and an opening extending laterally through a wall thereof proximate the distal end, the channel including a ramped surface along a distal portion thereof opposite the opening. The device further includes a wire extending along a longitudinal axis from a proximal end to a distal end, the wire sized and shaped to be inserted into the channel of the nail such that the distal end engages the ramped surface to extend through the opening.

Abstract: A system for treating a bone fracture includes an intramedullary nail sized and shaped to be inserted through a medullary canal of a bone to extend across a fracture site of the bone, the intramedullary device extending from a first end to a second end and including a plurality of openings extending laterally therethrough, the openings sized and shaped to receive bone fixation elements therethrough, and an insertion device including a base portion and a handle portion extending therefrom, the base portion integrally formed with the intramedullary nail and connected thereto via a plurality of connection points which, when a force is exerted thereon, break to disconnect the insertion device from the intramedullary nail, the base portion including a plurality of guide channels extending therethrough, each of the guide channels being aligned with a corresponding one of the openings of the intramedullary nail.

Abstract: In one embodiment a method of implanting a prosthetic includes implanting a first member including a concave articulation surface portion defined by a first radius of curvature in a first bone, implanting in a second bone a second member including a first convex articulation surface portion defined by a second radius of curvature and a second convex articulation surface defined by a third radius of curvature, wherein the second convex articulation surface is defined by the lemon portion of a spindle torus and each of the second radius of curvature and the third radius of curvature has a length that is different from the length of the first radius of curvature by less than 0.05 millimeters and wherein the origin of the second radius of curvature is not coincident with the origin of the third radius of curvature, and bringing the first member into slidable contact with the second member.

Abstract: Disclosed herein is a method of treating a patient that involves injecting a flowable material into a cancellous bone region of a bone, wherein the material is adapted to facilitate tissue regeneration, and then irradiating the cancellous bone region with an effective amount of NIR/red light. The irradiation may be carried out from a light source located inside the bone. The light may enter the bone via a transmitter located underneath the skin of the patient.

Abstract: This invention relates to an intervertebral motion disc having two motion surfaces and. wherein the radius of the upper articulation surface of the core member is greater than the radius of the lower articulation surface of the core member, and wherein the first articulation surface of the core member is spherical and the second articulation surface of the core member is curved and non-spherical.

Abstract: A soft tissue displacer tool can include a shaft that is elongate along a central axis, the shaft including a shaft body that defining a proximal end, a distal end that is spaced from the proximal end in a distal direction, and a central location that is disposed equidistantly between the proximal and distal ends. The shaft defines at least one inclined groove that 1) is inclined with respect to a plane that is normal to the central axis, and 2) revolves about the central axis, the groove terminating at a first end and a second end that is spaced from the first end along the distal direction, and the second end is spaced from the distal end. Soft tissue displacer tools are also described in which the shaft is cannulated. The soft tissue displacer tool can further include a guidance member, such as a K-wire, a trocar, or a bone punch.

Abstract: A secondary cover plate that contacts a stand-alone fusion cage without rigidly connecting to the cage, and instead only docks against the cage (or passes through a fixation cage) and is secured into the adjacent bone. The secondary cover plate is the last item that would be added to the fixation cage construct and would at least partially cover the head of one or more angled screws. The secondary cover plate could slidably engage the fixation cage without permanently snapping into any features of the cage itself. The secondary cover plate would then be final positioned by advancing into one or more adjacent vertebral bodies. The secondary cover plate advancing step could be achieved by tapping it into place (into bone) so that it is finally secured into the bone.

Abstract: A bone plate includes (a) a body having a first surface which, in an operative configuration, faces away from a bone on which the plate is to be mounted and a second surface, which in the operative configuration, faces the bone, the body including a first section extending along a first longitudinal axis and a second section extending along a second longitudinal axis angled with respect to the first longitudinal axis; (b) a first hole extending through the body from the first surface to the second surface and defining a first hole axis, the first hole being structured to lockingly engage a head of a first bone anchor inserted therein such that a shaft of the first bone anchor extends along the first hole axis; and (c) a second hole extending through the body and spaced apart from the first hole. The second hole defines a second hole axis and is structured to lockingly engage a head of a second bone anchor inserted therein such that a shaft of the second bone anchor extends along the second hole axis.

Abstract: An envelope for housing a medical device includes a body including first and second panels connected to one another along an edge thereof to define an interior space sized and shaped to house a medical device sealed within a packet and a first opening arrangement including a perforation extending about the body along the first and second panels to define a break portion breakable from a remaining portion of the body to open the envelope along with a second opening arrangement including a tab extending from a portion of the body such that pulling the tab in a direction away from the body tears a portion of the perforation extending along the first panel to open the envelope.

Abstract: The present invention provides a drug eluting surgical screw and a method for manufacturing a drug eluting surgical screw. The drug eluting surgical screw may include a shaft having a threaded portion, a head having a drive recess disposed at a proximal end of the shaft, the drive recess having a reservoir region and a driver engagement region, and at least one or more drug eluting components disposed within the reservoir region of the drive recess in a manner that does not substantially impair a connection between a driver and the surgical screw when the driver is operably disposed within the driver engagement region, each of the at least one or more drug eluting components including a carrier matrix and a therapeutic agent, the therapeutic agent being at least 20 wt % of the drug eluting component prior to any implantation of the drug eluting surgical screw.