Abstract: A surgical access device assembly that allows access to a pathology being treated while significantly reducing the risk of damaging anatomical structures proximate the pathology. The access device assembly includes a base portion having a central bore extending therethrough, and retractor blades pivotably mounted to the base portion. An insertion handle is coupled to the base portion to thread the retractor blades into the patient. The insertion handle is removed from the base portion, and a core hollow screw is threaded into the base portion to separate the retractor blades to gain access to the pathology through the hollow screw.

Abstract: A retractor device for cervical spinal fusion surgery. The retractor device includes a first post assembly having a first pin for mounting the first post assembly to a first vertebral body and a first rod coupled thereto in a multi-axial manner so that the first rod can be pivoted relative to the first pin. The retractor device also includes a second post assembly having a second pin for mounting the second post assembly to a second vertebral body and a second rod coupled thereto in a multi-axial manner so that the second rod can be pivoted relative to the second pin. The retractor device also includes a first retractor blade having a first retractor blade arm slideably engageable to the first rod, and a second retractor blade having a second retractor blade arm slideably engageable to the second rod. The first retractor blade is slid down the first rod and the second retractor blade is slid down the second rod to be positioned and separate the anatomical structures.

Abstract: A spacer device that is to be inserted between the spinous process of adjacent vertebrae. In one embodiment, the spacer device is percutaneously inserted between the spinous process of adjacent vertebrae using minimally invasive surgical procedures. The spacer device includes a body portion having a channel extending therethrough, a plate member attached at one end of the body portion that is larger cross-wise than the body portion, and at least one retaining member attached proximate to an opposite end of the body portion from the plate member. The spacer device is inserted between the spinous process with the retaining member stored within the body portion. A deploying device is inserted into the channel to deploy the retaining member to lock the spacer device in place.

Abstract: A method for providing disc regeneration that includes at least partially restoring disc height using a vertebral disc annular fibrosis tensioning and lengthening device, and then injecting a biologic substance, such as stem cells, into the disc that differentiate into chondrocytes and/or notochordal cells that facilitate disc regeneration. Once the biologic substance has regenerated the disc, it may be possible to remove the vertebral disc annular fibrosis tensioning and lengthening device.

Abstract: A surgical screw that includes a body portion that facilitates bone in-growth from a bone in which the screw is mounted so as to stabilize the screw in the bone. The body portion can have various configurations for facilitating bone in-growth, such as indentations, a roughened surface, such as by acid etching or abrasive media blasting, specialized coatings, such as hydroxyapetite, sintered beads, machined channels, etc. Because the body portion of the screw facilitates bone growth, the screw will be more firmly mounted to the bone so as to have a greater integrity in response to movement of the bone. The type of surgical screw can be any surgical screw that will benefit from being better anchored in bone, such as pedicle screws, long bone screws, cervical fusion screws, tendon anchoring screws, etc.

Abstract: A method for providing vertebral disc annular fibrosis tensioning and lengthening that restores the loss of disc height and provides disc regeneration. In one non-limiting embodiment, the method includes inserting pedicle screws into the vertebral bodies of adjacent vertebra and positioning a spring in compression between and in contact with the pedicle screws so that the spring bias forces the pedicle screws apart to provide a distractive force that increases the height of the disc space and promotes the disc regeneration.

Abstract: An interbody device that restores the disc space height between two vertebrae during spinal fusion surgery. The device includes a center plate surrounded by a perimeter portion that combine to have a relatively flat configuration in one dimension and relatively wide configuration in a perpendicular dimension. After the disc space has been cleared, the device is inserted into the disc space in a direction so that the wide dimension of the device is substantially parallel to the body of the vertebrae. The device is then rotated so that the wide dimension of the device becomes perpendicular to the vertebral body so as to cause the disc space height to be restored. Bone graft material is then introduced through a fill tube coupled to the device so that the bone graft material is distributed on both sides of the center plate and into the disc space.

Abstract: A minimally invasive interbody device assembly that includes an interbody device that restores the disc space height between two vertebrae and an instrument detachably coupled to the interbody device for positioning the device in the disc space and delivering bone material to the disc space that is distributed on both sides of the interbody device. The device is inserted into the disc space using the instrument in a direction so that the wide dimension of the device is substantially parallel to the body of the vertebrae. The device is then rotated by the instrument so that the wide dimension of the device becomes perpendicular to the vertebral body so as to cause the disc space height to be restored. Bone graft material is then forced down the instrument so that the bone graft material is distributed on both sides of the device. The instrument is then detached from the device.

Abstract: A vertebral disc annular fibrosis tensioning and lengthening device that restores the loss of disc height as a result of disc degeneration and other factors. The vertebral disc annular fibrosis tensioning and lengthening device includes pedicle screws having heads with cup-shaped cavities. The pedicle screws are threaded into the vertebral bodies of adjacent vertebrae through the pedicles so that open parts of the heads of the pedicle screws face each other. A spring is inserted into the cup-shaped cavities in compression so that the spring bias forces the pedicle screws apart, thus increasing the height of the disc space.

Abstract: An interspinous process spacer insertion device that positions an interspinous process spacer between the spinous process of adjacent vertebrae in a minimally invasive percutaneous surgical procedure. The device includes a trocar rod that extends through a cannulated sleeve. The spacer is attached to the end of the cannulated sleeve, where a trocar tip of the trocar rod extends through the spacer. The trocar rod is moved through the cannulated sleeve and an incision in the patient, and is positioned between the spinous process of the vertebra to align the device. The cannulated sleeve is then moved down the trocar rod so that the spacer slides between the spinous process, and the trocar rod is then withdrawn from the patient. The spacer is then rotated so that it locks behind the spinous process, and the cannulated sleeve is detached from the spacer and removed from the patient.

Abstract: A pedicle screw and rod system for minimally invasive spinal fusion surgery that allows for ease of placement of a fusion rod on the heads of pedicle screws. The system includes extender tubes having a bore extending therethrough. The bore includes a cylindrical portion and a key portion. A slot is formed in the tube along the length of the tube and is open to the bore. The pedicle screws are threaded into the vertebra and the extender tubes are coupled to the heads of the screws so that the slots face each other. The rod is positioned in the slots and is slid down the bores to be coupled to the heads of the pedicle screws. Bolts are slid down the tubes and threaded to the heads of the pedicle screws to secure the rod thereto, and the extender tubes are removed.

Abstract: A disc space preparation device that has particular application for removing disc material during spinal fusion surgery. The disc preparation device includes a body portion that houses a motor having a shaft attached thereto that is rotated by the motor. The shaft extends through a chamber in a neck portion of the device and into an open head portion of the device at the end of the neck portion opposite to the housing. The head portion rotates relative to the neck portion. The head portion includes a series of blades that are used to cut-away the disc material. The shaft includes an auger that draws the cut material through the neck portion. A suction port is coupled to the chamber in the neck portion to remove the disc material therefrom.

Abstract: A surgical delivery system that has particular application for providing bone graft material to an interbody device that restores disc space height during spinal fusion surgery. The bone graft delivery system includes a body portion and a shaft coupled thereto. An auger extends through a bore in the shaft and into the body portion. An end of the shaft opposite to the body portion is configured to be coupled to the interbody device, where the auger extends through a channel in the interbody device. Bone graft material is placed in a hopper coupled to the shaft, where the auger is manually or automatically rotated to deliver the bone graft material through the shaft and into the interbody device where it is dispersed into the disc space.

Abstract: A method for providing an InVivo model of disc degeneration. The method includes percutaneously inserting a needle into a non-human surrogate disc, generally the disc of a rabbit, so that the needle ruptures the annulus of the disc. Fluoroscopy X-ray images can be used to visualize the placement of the needle to the proper location. By using the proper surrogate, rupture of the annulus of the disc will have a quick degenerative effect on the disc, which can be visualized using MRI or other suitable imaging devices. By studying the etiologies associated with disc degeneration of the surrogate, treatments can then be devised to attempt to reduce the rate of degeneration, reverse degeneration, or other disc treatment procedures.

Abstract: A protective lead shield for use during spinal surgery. The lead shield is intended to be draped over the back of a patient lying in the prone position during the surgical procedure. The lead shield includes a central opening that is positioned over the pathology being treated so as to allow the surgeon to gain access thereto with various surgical devices. The lead shield has an hour-glass shape where a narrow part of the shield is aligned with the opening. The wider ends of the shield allow the shield to be maintained in place on the patient, and the narrow part of the shield and the opening allow fluoroscopic X-rays to be taken of the spinal area being treated from both the top and the side. Thus, the surgical procedure can be effectively performed, the surgical area can be effectively X-rayed and the surgeon can be effectively protected from X-rays while the shield is in place.

Abstract: A pedicle access device that has particular application for positioning a pedicle screw during a minimally invasive spinal fusion surgical procedure. The pedicle access device includes a positioning needle having a hollow tube and a specially designed tip that conforms with a facet complex of a vertebra proximate a pedicle. A targeting needle having a pointed end is inserted through the hollow tube of the positioning needle, and is secured thereto so the tip of the targeting needle extends out of the end of the positioning needle. The tip of the targeting needle allows the positioning needle to be accurately positioned on the pedicle, and the specially configured tip of the positioning needle allows it to be secured thereto without slipping.

Abstract: A collection device for collecting bone material during a spinal fusion surgical procedure so that the bone material can later be used as a graft material for the fusion procedure. The device includes a container that collects the bone and other material that is removed from the patient during the surgical procedure through a suction hose. The device includes a plunger having a filter plate sealed to the inside of the container. The plunger is pushed down into the collected material in the container so that blood and other liquids are forced through the plate to be separated from the bone material. A cover at the bottom of the container can be removed to remove the collected bone material.