Abstract: An expandable access device for providing access to a surgical site in the body. The expandable access device comprises a first blade, a second blade and a connection mechanism operable connecting the first and second blades. Each blade may have a first portion, a second portion and an intermediate portion between the first and second portions. The intermediate portions of each blade may be bent such that the first and second portions of each blade may be at an angle with respect to each other. The connection mechanism may have first and second elongated member, which may be in a criss-cross configuration. A first end of the first and second elongated members may be connected to the first blade and a second end of the first and second elongated members may be connected to the second blade. Such a construction may enable the first and second blades to separate and pivot with respect to each other.

Abstract: The invention relates to an artificial intervertebral disc for placement between adjacent vertebrae. The artificial intervertebral disc is preferably designed to restore disc height and natural disc curvature, allow for a natural range of motion, absorb shock and provide resistance to motion and axial compression. Furthermore, the intervertebral disc may be used in the cervical, the thoracic, or the lumbar regions of the spine. The artificial intervertebral disc may include either singularly or in combination: an interior including at least one spring member preferably incorporating a arcuate surface member, a flexible core, the flexible core preferably being a slotted core, a ring spring, a winged leaf spring, or a leaf spring, or The articulating member preferably being attached to one of the endplate by an intermediate shock absorbing element.

Abstract: The invention relates to an artificial intervertebral disc for placement between adjacent vertebrae. The artificial intervertebral disc is preferably designed to restore disc height and lordosis, allow for a natural range of motion, absorb shock and provide resistance to motion and axial compression. Furthermore, the intervertebral disc may be used in the cervical, the thoracic, or the lumber regions of the spine. The artificial intervertebral disc may include either singularly or in combination: an interior at least partially filled with a fluid; a valve for injecting fluid into the interior of the disk; a central region having a stiffness that is preferably greater than the stiffness of the outer regions thus enabling the disc to pivot about the central region. The central pivot may be formed by a center opening, a central chamber, an inner core or a central cable.

Abstract: A depth gauge for measuring the depth of blind holes in bones and/or nails inserted into bones is provided. The tool includes a probe with an abutment at its end to engage against the distal edge of the blind hole; a tubular body; and a grooved insert. After the probe, slidably disposed within the tubular body, is positioned through the blind hole to be measured, the grooved insert is slid forward inside the tubular body, surrounding the probe, and pushing the probe sideward, towards the blind hole wall. When probe and groove insert are retracted together, they firmly engage against the distal bone wall. The tubular housing is then pushed forward until it abuts against the proximal bone wall, allowing even in small diameter holes, an accurate reading of hole depth on the scale located at the rear end of the probe.

Abstract: An implant, in particular an intervertebral implant, comprising (A) two articulating parts (4; 5) having each a central axis (1; 26), each a curved slide surface (6; 7) intersecting the central axes (1; 26), and each an axially outermost end (14; 15) that can be connected to a bone, where (B) the slide surfaces (6; 7) are curved and displaceable one on the other, where (D) the second articulating part (5) is rotatable about two mutually skewed axes of rotation (10; 11) relative to the first articulating part (4).

Abstract: An external midface distractor is disclosed for attachment to the bones of a patient's cranium and midface region for performing an osteogenesis procedure to gradually lengthen a portion of the craniofacial skeleton. The midface distractor generally includes an external halo assembly for engaging the patient's cranium, a central adjustment assembly, a vertical central rod, at least one horizontal cross piece assembly including at least one distraction screw, and at least one bone engaging portion which is mounted to the targeted facial bone to be distracted. The midface distractor may also include various individual adjustment mechanisms that provide surgeons greater and more precise control over the distraction vector than is available with current devices. That is, the midface distractor may provide surgeons with additional anterior-posterior and medial-lateral adjustments, thus permitting surgeons to more precisely and accurately control the direction of distraction.

Abstract: Methods and apparatus provide for: coupling an elongate guide substantially at a first end to at least one vertebral body of a spinal column of a patient; and extending a second end of the guide to a structure of the patient spaced in an anterior direction away from the at least one vertebral body towards an entry incision.

Abstract: An assembly for use with a bone fastener includes a fixation device and a bone fastener retainer device. The fixation device has an opening configured to receive a bone fastener in an installed position in which an outer end portion of the bone fastener is located within the opening. The retainer device is receivable over the fixation device in a closed position extending over the location taken by the outer end portion of the bone fastener within the opening. Additionally, the fixation device and the retainer device together have first and second locking structures. The locking structures are configured to engage each other in an undeflected condition when the retainer device is in a partially closed position, and to snap into interlocked engagement with each other under an applied force that moves the retainer device from the partially closed position to the closed position.

Abstract: The invention relates to dura substitutes to be used as prostheses for dural defects in the field of neurosurgery and processes for producing the same. The present invention provides artificial dura mater materials comprising sheets of microbial-derived polysaccharide processed to have the necessary strength characteristics, conformability and physical properties.

Abstract: The present invention relates to a transbuccal plate holding cannula used in osteofixation procedures. The transbuccal plate holding cannula of the present invention can be releasably secured to a bone plate such that tools and fasteners may be passed through the plate holding cannula in order to secure the bone plate to a bone.

Abstract: An apparatus for use with bone fasteners comprises a first fixation device having a slot configured to receive a bone fastener, and a second fixation device having another slot configured to receive another bone fastener. The first and second fixation devices are interconnected for rotation relative to each other when the bone fasteners are in the slots. Summarized differently, an apparatus for use with bone fasteners comprises a first fixation device having a first pair of openings defining bone fastener locations, and a second fixation device having a second pair of openings defining bone fastener locations. The first and second fixation devices are interconnected for movement relative to each other such that the bone fastener locations defined by the first and second pairs of openings are located at four corners of a rectangular array.

Abstract: The present invention relates in general to implantable compositions, and method for preparing same, containing a calcium salt-containing component, optionally demineralized bone, a plurality of discrete fibers, optionally a flow additive, and optionally continuous reinforcing fibers or an array of organized fibers in the form of mesh. Advantageously, the discrete fibers have a specific aspect ratio (length/diameter) from about 50:1 to about 1000:1. The addition of a small amount of discrete fibers and/or the continuous reinforcing fibers or fiber mesh can cause drastic increases in certain mechanical properties including flexural strength, flexural toughness, and/or screw pullout strength.

Abstract: A surgical instrument is provided for urging a longitudinal spinal member into a top-loading spinal implant. The instrument may comprise a holder assembly having a pair of fingers sized and configured to engage the underside of an edge of the spinal implant, a release assembly, and an actuating member. The release assembly may comprise a tubular member and a pusher member, the tubular member being sized and configured to be slidably disposed within the holder assembly, and the pusher member being sized and configured to slidably surround at least a portion of the holder assembly. Upon movement of the actuating member, the holder assembly and the release assembly are moveable with respect to one another so that the longitudinal spinal rod, which is engaged to the pusher member, is urged into engagement with the rod-receiving channel of the spinal implant.

Abstract: An allogenic implant for use in intervertebral fusion is formed from one or more two pieces. The pieces are made from bone, and are joined together to form an implant having sufficient strength and stability to maintain a desired distance between first and second vertebrae in a spinal fusion procedure. The implant pieces may be formed of cortical bone and connected by dovetail joints, and at least one cortical bone pin may be provided to lock the pieces together and to add strength to the implant. Teeth are formed on the vertebra engaging surfaces of the implant prevent short-term slippage of the implant.

Abstract: A surgical drill guide for use with a bone plate having fastener holes oriented at predetermined angles with respect to the plate, the surgical drill guide having at least one alignment drill guiding barrel that is aligned with the respective fastener holes in the bone plate for drilling the holes at the desired range of angles permitted by the plate hole.

Abstract: A device for treating bone fractures and/or for fixing surgical implants, surgical threads or tissues in or on the bone comprising a closing element and a rivet. The rivet includes a shaft extending from a rear end to a front end coaxial to a central axis and having a through-hole extending coaxially therethrough. The shaft of the closing element is coaxially displaceable in the through-hole and the head of the closing element can be axially brought to rest on the front shaft end. The rivet also comprises at least two grooves on the outside, these grooves extending from the front shaft in the direction of the rear end, parallel to the central axis.

Abstract: An external midface distractor is disclosed for attachment to the bones of a patient's cranium and midface region for performing an osteogenesis procedure to gradually lengthen a portion of the craniofacial skeleton. The midface distractor generally includes an external halo assembly for engaging the patient's cranium, a central adjustment assembly, a vertical central rod, at least one horizontal cross piece assembly including at least one distraction screw, and at least one bone engaging portion which is mounted to the targeted facial bone to be distracted. The midface distractor may also include various individual adjustment mechanisms that provide surgeons greater and more precise control over the distraction vector than is available with current devices. That is, the midface distractor may provide surgeons with additional anterior-posterior and medial-lateral adjustments, thus permitting surgeons to more precisely and accurately control the direction of distraction.

Abstract: A novel coplanar X-ray guided method and aiming arm device for insertion of distal locking screws in intramedullary bone nails. Radiopaque target markers in the aiming arm enable the easy positioning of an X-ray source such that an X-ray beam is coplanar with the aiming arm transverse holes. After the X-ray source is accurately oriented, a single X-ray snapshot is enough to assess the exact distortion of the implanted intramedullary nail. The X-ray beam need not be coaxial with the nail holes. The aiming arm includes a mobile portion and a fixed portion fastened to the nail, and the aiming arm can be adjusted, displacing the mobile portion over the fixed portion, to compensate for the distortion of the intramedullary nail caused by implantation in bone.

Abstract: A fixation assembly is described, comprising a fixation plate having an upper surface, a lower surface, a longitudinal axis, and a first opening extending from the upper surface through to the lower surface; a first resilient element extending through at least a portion of the first opening; wherein the first opening is configured to receive a first bone fastener, the first bone fastener having a head and a shaft; wherein the first resilient element is deflectable from a first condition to a second condition; and wherein the first resilient element is configured to engage at least a portion of the head of the first bone fastener when the first bone fastener is at least partially inserted into the first opening. A method of use is also described.

Abstract: A retractor with multiple blades for use in surgery. The retractor may comprise first and second elongated portions which are pivotally connected to each other. A first blade may be connected to the first elongated portion and a second blade may be connected to the second elongated portion. The retractor may also comprise a sliding bar having a third blade. The sliding bar may be associated with the first and second elongated portions such that movement of the elongated portions relative to each other may result in movement of the sliding bar and, consequently, movement of the third blade relative to the first and second blades. In one embodiment, the retractor may comprise a tension limiting device so that the third blade may remain relatively stationary as the first and second blades are moved. The retractor may also comprise a fourth blade operatively connected to the first and second elongated portions. The fourth blade may be moved independently of the other blades or may move with the other blades.