Abstract: Systems and methods for treating vertebral compression fractures are provided. A kit can include at least one body containing a bone cement precursor to be mixed with at least one other bone cement precursor to form a bone cement. The body or a package containing the body can include at least one sensor. In some embodiments the sensor can be a temperature sensor. In some methods, data from the sensor can be used to determine certain parameters related to a treatment interval involving the bone cement.

Abstract: A fracture reduction implant for treating a vertebral compression fracture and instruments and methods for implanting the fracture reduction device utilizing a minimally invasive lateral approach are described. The implant may be inserted into a fractured vertebra through a T-shaped cut formed in the vertebral wall. The T-shaped cut may be formed in the lateral aspect of the wall. After insertion, a portion of the implant may be elevated within the vertebral body to reduce the fracture. The implant may include a base assembly, elevator plate, and a support column. The support column may be locked to the base assembly after insertion.

Abstract: Embodiments relate to implantable devices for the treatment of syndesmosis injuries. Embodiments include a first anchor attachable to a first bone, the first anchor being coupled to a flexible component, the flexible component in turn being coupled to a base component. The base component may be rigid, and may be externally threaded for engaging with a second anchor. Position of the second anchor may be adjusted by rotating the second anchor with respect to the base component, thereby adjusting relative position of the two bones. An assembly may be created in which an outer tube contains the flexible component and the base component inside the outer tube, and at its distal end the outer tube may engage the first anchor so as to allow transmission of torque. The outer tube may be withdrawn proximally after implantation of the first anchor. The bones may be a tibia and a fibula.

Abstract: An ear speculum that includes a body having an ear-contacting tip with an opening; a light providing member; a viewing member; and a vacuum intake port, wherein the members and intake port are provided within the ear speculum with the vacuum intake port occupying a larger portion of the of the cross-sectional area of the ear speculum opening than the light providing or viewing members to facilitate removal of material from an ear canal. Also, an otoscope that includes a head; an ear speculum as described herein in operative association with the head; an image detector in image communication with the viewing member; a suction source in vacuum communication with the vacuum intake port; and a light source in illumination communication with the light providing member. Also, a system and method for removing material or debris from an ear canal using the otoscope described herein.

Abstract: A surgical instrument has first and second components that can rotate relative to one another and a locking mechanism to selectively restrict or allow rotation between the first and second components. One component has a first array of two or more grooves or teeth spaced apart at a first angular pitch and at least one further groove or further tooth which does not correspond to the first angular pitch. The other component comprises a first tooth or a first groove to engage one of the first array of grooves or teeth to selectively restrict rotation to two or more predetermined rotational positions; the other component also selectively engages the at least one further groove or further tooth on the first component to selectively restrict rotation between the first and second components at a 0° rotational position.

Abstract: A spinal implant. The spinal implant includes a spacer having an upper surface for contacting a superior vertebral body, a lower surface for contacting an inferior vertebral body, a first insertion end portion, and a second end portion opposite the first insertion end portion; a fixation frame coupled to the second end portion of the spacer and including a bridge portion oriented substantially coplanar with the spacer and at least one arm extending from the bridge portion; and at least one fixation element having a first insertion end for penetrating the superior or inferior vertebral bodies and a second end coupled to the at least one arm of the fixation frame.

Abstract: A bone fastener for use in orthopedic surgery for fixing an implant to bone has a threaded or unthreaded shaft configured to engage bone and a head having a thread on an outer surface to engage the implant. The thread on the head of the fastener has a profile in cross section that includes arcuate peaks with a flat on the outer surface of the peak.

Abstract: An interbody spacer includes an elongated body with a maximum width between opposite side walls and a maximum height between upper and lower bearing surfaces. The interbody spacer also includes a leading end nose connecting the side walls to facilitate insertion of the interbody spacer into a disc space between vertebrae in an insertion orientation, from which the interbody device is then rotated to position the upper and lower bearing surfaces in contact with the endplates of the adjacent vertebrae. The leading end nose forms a blunt convex nose between the upper and lower bearing surfaces to maximize the bearing surface area available to contact the adjacent endplates.

Abstract: A trial system for an implantable joint replacement includes a guide assembly having a baseplate and a guide plate, the guide plate rotatable relative to the base plate about a rotation axis extending through the guide plate and the baseplate while directly connected to the baseplate. An adjustment mechanism is actuable to selectively control the rotational juxtaposition of the guide plate relative to the baseplate. The rotation axis may be medially offset from the center of the guide assembly. A single instrument may be used to rotate the guide plate relative to the base plate and lock the plates in the selected juxtaposition. The guide plate provides in situ positionable cutting guidance for implantation of prosthetic joint components. The system may further include an articulating insert trial mounted on the guide assembly to determine preferred joint alignment and/or optimal positioning of the guide plate.

Abstract: A drill bit (1) has a central axis (A) and a tapered cutting end part (2 ) terminating in a drill tip (3) at one end of the drill bit (1), a shank (4) extending from an opposing end of the drill bit (1), and a body (4a) extending between the cutting end part (2) and the shank (4). A plurality of flutes (5) are formed in the drill bit (1) and helically extend along the body (4a) into the cutting end part (2). Each flute (5) has a flute leading side wall (6) and a flute trailing side wall (7). A land (9) is defined on the body (4a) between each of the flutes (5) and extends to the cutting end part (2). In any body cross-sectional plane extending perpendicular to the central axis (A) through the body (4a), a land leading edge region (11) of each land (9) adjoining the flute trailing side wall (7) of a leading adjacent flute (5) is convexly curved.

Abstract: A bone screw driving system includes a screw having a head and a shaft extending from the head. The screw includes a stepped opening extending in the shaft that includes a first portion and a second portion having a greater cross-sectional dimension than the first portion. The bone screw driving system further includes a screw driver having a driver shaft that defines a tip configured to engage the screw head. The driver further includes a pin extending from the tip and sized to fit within the opening. The pin includes an abutment movable to a locked configuration in the second portion of the opening, wherein the abutment defines a cross-sectional dimension greater than that of the first portion of the opening.

Abstract: Orthopedic plating assemblies and methods for bone fixation that include an orthopedic plate and orthopedic anchors that can accommodate subsidence in the vertebral bodies as well as prevent the anchors from “backing out” of their installed position. The orthopedic anchors may be capable of rotating and translating with respect to the plate, and the plate may be able to translate after being fastened to the vertebral bodies.

Abstract: A surgical access assembly for positioning within an opening in tissue including an outer frame positionable outside a patient and defining an opening therein dimensioned to receive a surgical instrument therethrough. The outer frame includes first and second portions. The first portion is biased into locking engagement with the second portion such that a first engagement structure is in locking engagement with a second engagement structure. An inner member is positionable within a patient and a flexible member extends between the inner member and outer member and is operatively associated with the outer member. The first portion is movable to overcome the bias to move the first and second engagement structures to a disengaged position, wherein in the disengaged position at least one of the first and second portions is movable with respect to the other portion to adjust the tension on the flexible member to retract tissue.

Abstract: A reinforced access assembly is provided. The access assembly includes a compressible body having proximal and distal ends and a substantially hourglass-shaped central portion extending therebetween. The compressible body defining at least a first lumen configured to receive an instrument in a sealing manner. The access assembly further includes a reinforcing mechanism extending between the proximal and distal ends of the compressible body. The reinforcing mechanism includes a plurality of rib members configured to permit compression of the compressible body during insertion into an incision and return the compressible body to an uncompressed condition following insertion.

Abstract: The present invention is a method and device for the correction and reduction of bone deformities, such as metatarsus primus adductus, using a plate body with winged buttresses and dorsal loop. The method and device can be affixed to a bone without any drilling or violating of the bone and can use a tethering technique which does not require drilling into the second metatarsal, nor does it require the placement of a prominent suture knot/button device medially along the first metatarsal.

Abstract: The present invention is a self-locking internal adapter for D-shaped orthopedic tools. A locking ball mechanism prevents movement of the adapter components relative to each other, while a plurality of securing ball mechanisms releasably secure a D-shaped orthopedic tool in the adapter. A chamfered surface of the adapter engages a chamfer of the tool to centrally stabilize the tool in the adapter. The internal adapter may be used with driver handles, ratcheting handles and torque-limiting handles.

Abstract: Plate devices are provided for mounting to bone and receiving one or more spinal rods. The devices may include coupling members or rod receiving members coupled to the plate member and configured to have multiple degrees of adjustability in order to accommodate elongate connecting members of various orientations. The plate devices may also include quick locking features or locking devices that secure multiple points of articulation simultaneously.

Abstract: The invention provides systems and methods for sternum repair. A sternum repair device may include a central body, which may include a plurality of bands and buckles, such that a band extends from the central body and is received by a buckle component. The band may wrap around the sternum and the device may be tightened to keep the separate sternum pieces together.

Abstract: A surgical retractor and a method of minimally invasive surgery, wherein the surgical retractor includes ribs and a mechanism for microns-resolution transferring of linear and rotational movements of the ribs and wherein each rib can be easily replaced without use of any additional tools. According to an embodiment of the present invention the transmission is simpler. Likewise, an auxiliary handle is added to facilitate the insertion of the ribs into the body of the operated patient, and the vast majority of components of the surgical retractor are made with biocompatible, and FDA approved material ULTEM HU 1000 RESIN transparent (radiolucent) to X-ray radiation and are designated for single use.

Abstract: In at least one embodiment of the present invention, a device for mixing and dispensing a bone cement mixture is provided. The device comprises a first chamber and a second chamber. The first chamber is for containing a first bone cement component. The second chamber is for containing a second bone cement component. A valve is in fluid communication with the first and second chambers. A first and a second plunger are respectively within the first and second chambers and are configured to actuate within their respective chambers. When the valve is in a first position actuating the first plunger advances the first bone cement component into the second chamber to form the bone cement mixture.