Abstract: An orthopedic device for implanting between adjacent vertebrae comprising: an arcuate balloon and a hardenable material within said balloon. In some embodiments, the balloon has a footprint that substantially corresponds to a perimeter of a vertebral endplate. An inflatable device is inserted through a cannula into an intervertebral space and oriented so that, upon expansion, a natural angle between vertebrae will be at least partially restored. At least one component selected from the group consisting of a load-bearing component and an osteobiologic component is directed into the inflatable device through a fluid communication means.

Abstract: An apparatus for dispensing a plurality of implants including a barrel, a magazine, and a driver. The barrel has a longitudinal passage and a lateral passage intersecting the longitudinal passage adjacent a distal end of the barrel. The magazine has a housing defining a chamber for holding a plurality of implants. The housing is slidably connected to the barrel and movable between a retracted position and an extended position wherein a slot of the housing is aligned with the lateral passage of the barrel. A pusher member connected to the housing is caused to push one of the implants through the slot and the lateral passage and into the longitudinal passage. The driver is disposed in the longitudinal passage to be axially and rotatably movable to apply a rotational force to the implant.

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 method of regulating a setting time of a bone filler material, the method comprising: (a) combining at least two filler material components to form a biocompatible mixture; (b) choosing a setting time for the mixture; and (c) regulating a temperature of the mixture to influence reaction kinetics so that the mixture does not set before the chosen setting time.

Abstract: An implant includes a body sized and shaped for insertion into a facet joint, the implant including a first bone fixation element receiving opening extending through a portion thereof along a first axis oriented so that, when the implant is received within a facet joint in a desired configuration, a bone fixation element inserted into the first bone fixation element receiving opening will extend into a first one of the vertebra forming the facet joint.

Abstract: A method for augmenting a tissue including introducing into the tissue a first thermoplastic material at a first condition; treating the first thermoplastic material to achieve a second condition that includes an at least partially crystalline skin; and introducing a second material into the tissue whereby the first thermoplastic material and the second material are contained by the at least partially crystalline skin. Also a method of fracture reduction in a tissue including exposing to gamma radiation a mass of polycaprolactone characterized by a first shape; heating the mass of irradiated polycaprolactone above its melting temperature; introducing the heated mass of polycaprolactone into the tissue annulus to deform it from the first shape; allowing the material to return to the first shape.

Abstract: An embolic device deployment system includes a catheter having a first lumen and proximal and distal ends. A notch is disposed in the first lumen, forming a second lumen. An embolic device has a retaining ring at the proximal end. An engagement member includes a distal loop extending through the retaining ring, and a proximal loop extending into the first lumen. An elongated detachment member can be disposed through the loops and have a detachment member bump disposed between the loops. When the detachment member is disposed within the distal loop and the distal loop is disposed within the retaining ring, the embolic device is engaged. When the detachment member is pulled proximally, the detachment member is withdrawn from the distal loop, and the detachment member bump contacts the proximal loop. These acts assist in the disengagement of the distal loop from the retaining ring to release the embolic device.

Abstract: A tissue manipulation system includes Programmable Markers configured to be implanted on opposite sides of one or more portions of tissue within a patient's body, Markers communicating with one another to enable a determination of their relative positions and External Device receiving and transmitting signals to Markers containing information as to Marker's positions. Device is configured to: capture an image of the tissue portions with Markers; manipulate the image of the tissue portions in a virtual environment or a simulated environment to a desired restored orientation; determine desired positions Markers will have when the tissue portions are in the desired restored orientation; program implanted Markers with the desired orientations.

Abstract: Various exemplary methods and devices are provided for fixing bone anchors to bone. In general, the methods and devices can allow for a bone anchor to be fixed to a bone at a desired angle to a receiver member. In an exemplary embodiment, a bone anchor assembly is provided that includes a bone anchor configured to engage bone, a receiver member that polyaxially seats a spherical head of the bone anchor, and a compression member seated within the receiver member, proximally of the head of the bone anchor. The compression member can have a distal end with gripping features thereon configured to create at least one line contact and/or one band contact with the head of the bone anchor, thus providing a firm grip on the head of the bone anchor and reducing a risk of slippage of the bone anchor with respect to the receiver member.

Abstract: A soft tissue fixation assembly includes a plurality of deformable bone anchors and a suture that is configured to fixedly attach to each of the bone anchors. One or more of the bone anchors can be inserted into a bone, and one or more of the bone anchors can be inserted through soft tissue and into the bone. The suture can be inserted through the bone anchors, and energy can be applied to the anchors, thereby causing a deformable material of the bone anchors to deform, thereby capturing the strand of suture in the bone anchor. The strand of suture can be placed in tension, and can extend over the soft tissue so as to retain the soft tissue in contact with the bone.

Abstract: A method includes inserting a stem into a bone, positioning a solid articulating portion of a mounting element within a tapered bore so that the mounting element is substantially free to pivot in multiple degrees of freedom relative to the stem while maintaining substantially contiguous engagement between the solid articulating portion and a portion of a surface of the tapered bore defining a circle, engaging the joint component to the mounting element, manipulating the mounting element to vary an angular position of the joint component with the mounting element positioned in the tapered bore while maintaining the substantially contiguous engagement, and mechanically locking the solid articulating portion in the tapered bore to fix a position of the mounting element relative to the stem after manipulating the mounting element by forcing the solid articulating portion toward a bottom of the tapered bore.

Abstract: An anchoring device includes (a) a flexible member extending from a proximal end to a distal end and (b) an elongated anchor member extending from a first end to a second end and attached to the distal end of the flexible member such that the anchor member is movable between an insertion configuration in which the anchor member is substantially parallel to the flexible member and a locked configuration in which the anchor member is substantially perpendicular to the flexible member in combination with (c) a flexible removal element extending from a proximal end to a distal end attached to the first end of the anchor member.

Abstract: A burr attachment designed for use with a curved burr attachment or other chuck attachments that includes a tube with a wire shaft supported therein and a coil spring surrounding said wire shaft and having each of the coils touch the outer periphery surface of the wire shaft and the inner peripheral surface of said tube to enhance cooling of said outer periphery of said tube from the heat generated by said wire shaft and attenuate vibrations while allowing said burr attachment to be bent without kinking.

Abstract: Embodiments of a hybrid imaging sensor that optimizes a pixel array area on a substrate using a stacking scheme for placement of related circuitry with minimal vertical interconnects between stacked substrates and associated features are disclosed. Embodiments of maximized pixel array size/die size (area optimization) are disclosed, and an optimized imaging sensor providing improved image quality, improved functionality, and improved form factors for specific applications common to the industry of digital imaging are also disclosed. Embodiments of the above may include systems, methods and processes for staggering ADC or column circuit bumps in a column or sub-column hybrid image sensor using vertical interconnects are also disclosed.

Abstract: Instrumentation and methods of use are provided for a medical device identification system. The application describes embodiments of a system including a medical device, and an identification tag having an RFID chip and an electrical circuit. The system defines a first configuration in which a first attachment region of the electrical circuit is in electrical communication with a second attachment region of the electrical circuit, and a second configuration in which the first attachment region is electrically isolated from the second attachment region. When the system is in the first configuration the RFID chip is in a first state, and when the system is in the second configuration the RFID chip is in a second state different than the first state.

Abstract: An interspinous spacer assembly for insertion and/or implantation between spinous processes of adjacent superior and inferior vertebrae includes an interspinous spacer member sized and configured for insertion into the interspinous space located between adjacent spinous processes and an engagement mechanism for operatively coupling the spacer member to the adjacent spinous processes and for preventing migration of the assembly once implanted. The interspinous spacer assembly is adjustable to conform to the individual anatomy of a patient's spine.

Abstract: Several devices and methods for preparing the vertebral endplates while minimizing damage to the vertebral endplates. Each design incorporates flexible means to reduce endplate damage while enabling removal of the cartilage adhered to the endplate cortical bone.

Abstract: A flexible chain implant for insertion into an interior volume of a vertebral body. The implant may be implanted in an insertion position for sliding through a cannula and is flexible for packing into the interior volume in an implanted configuration. The implant randomly separates in the implanted configuration. The implant includes a top member and a bottom member, wherein the top and bottom members are coupled to one another at a coupled portion. The top and bottom members preferably each include an inner surface such that the inner surfaces include a plurality of alternating projections and recesses so that the projections are received within the recesses in an insertion position. Alternatively, the implant may include a plurality of substantially non-flexible bodies and a plurality of substantially flexible links interconnecting the bodies. The non-flexible bodies include a plurality of facets and/or abutment surfaces.

Abstract: An intervertebral prosthesis or disk prosthesis comprising a front side, a rear side, an upper side which can be placed on the base plate of vertebral body, a lower side which can be placed on the base plate of a vertebral body, a right side, a left side, a cavity which can receive a fluid hydraulic osteocementum, an opening in the cavity and several outlets out from the cavity. The total of the transversal surfaces of the outlets SV on the front side, the total of the transversal surfaces of the outlets SH on the rear side, the total of the transversal surfaces of the outlets SR on the right side and the total of the transversal surfaces of the outlets on the left side satisfy the following conditions: SL>SR or SR>SL or SH>SV or SV>SH.

Abstract: A braided stent system includes an expansion ring attached to internal and external surfaces of a lumen. A frame of the ring may impart an outwardly expanding radial force to the lumen, the frame including a plurality of elongate members joined at a coupling and at first and second intersections opposite the coupling. A clip can extend from the intersections and can be operable to slidably secure the frame to the inner and outer surfaces of the lumen.