Abstract: A device, system and method for securing a plate to a bone. An anchor device has a screw (with a head portion) and a locking disc. The head portion includes a slotted wall defining a plurality of petals disposed around a central opening. The screw further includes an internal bore. The locking disc is rotatably disposed within the central opening, such that in a first rotational position the petals may flex inwardly, and in a second rotational position the petals are substantially prevented from flexing inwardly. A tool for manipulating the anchor device has a shaft with its end configured to mate with the internal bore of the screw to permit selective rotation of the screw, and a sleeve member rotatably and slideably mounted on the shaft having an end that mates with the locking disc to permit selective rotation of the disc.

Abstract: A device for attaching connective tissue to bone has a longitudinal axis and comprises an annular toggle member and a body member disposed distally of the toggle member, such that there is an axial space between the toggle member and the body member. The toggle member is movable between an undeployed position wherein the toggle member has a smaller profile in a direction transverse to the axis and a deployed position wherein the toggle member has a larger profile in the direction transverse to the axis. When installed in a desired procedural site, in suitable bone, suturing material extends axially through a center aperture in the annular toggle member, without being secured to or contacting the toggle member. This approach permits a suture attachment which lies entirely beneath the cortical bone surface, and which further permit the attachment of suture to the bone anchor without the necessity for tying knots, which is particularly arduous and technically demanding in the case of arthroscopic procedures.

Abstract: An anchor for fixing a ligament or tendon replacement in a bore formed in a bone has two parts. A first partially cylindrical part has a semi-circular bore therethrough extending along an axis. The bore tapers conically inwardly with respect to the axis from a larger radius at a first end to a smaller radius at second end. The outer surface of the partially cylindrical part is spaced at a constant radius from the axis between the first and second ends. The first and second parts have side walls formed between the bore and the outer surface which walls extend along a plane which forms an angle with respect to the central axis. When the two parts are engaged along their side wails and slide with respect to the axis the outer diameter of the two parts enlarges.

Abstract: This document discusses, among other things, fiducial marker devices, tools, and methods. One example illustrates a combined computed tomography (CT) imagable fiducial locator head, an integral bone screw, and an integral divot for receiving a positioning wand of an image-guided surgical (IGS) workstation. A further example includes a fluid/gel-absorbing coating or cover into which a magnetic resonance (MR) imagable fluid is introduced, thereby permitting both CT and MR imaging. Protective caps and collars may be used to protect the fiducial marker from mechanical impact and/or to guide the fiducial marker during affixation. A bull's-eye or other template is used to select a center of a substantially spherical fiducial marker head on an image, such as for use during patient registration.

Abstract: An innovative bone anchor and methods for securing soft tissue, such as tendons, to bone, which permit a suture attachment that lies entirely beneath the cortical bone surface. Advantageously, the suturing material between the soft tissue and the bone anchor is secured without the need for tying a knot. The suture attachment to the bone anchor involves the looping of a length of suture around a pulley within the bone anchor, tightening the suture and attached soft tissue, and clamping the suture within the bone anchor. The bone anchor may be a tubular body having a lumen containing a plurality of suture-locking elements that clamp the suture therein. The locking elements may be thin and C-shaped. One or more locking plugs attached to separable actuation rods displace axially within the lumen and act on the locking elements to displace them radially.

Abstract: A system for securing a graft within a bone includes a tubular cross pin having an interior surface bounding a passageway extending between a proximal end and an opposing distal end, the distal end terminating at a distal end face. A guide pin has an exterior surface extending between a proximal end and an opposing distal end, the exterior surface including an outwardly projecting shoulder. The guide pin is removably received within the passageway of the cross pin such that the distal end face of the cross pin biases against the shoulder and a proximal portion of the guide pin freely projects beyond the proximal end of the cross pin.

Abstract: An adapter including a coupling portion defining a lumen to receive a pedicle post, an intermediate portion including a first end fixedly attached to a side of the coupling portion and including a second end distal from the coupling portion, and a bolt. A proximal end of the bolt is rotatably coupled to the second end of the intermediate portion and a distal end of the bolt includes a connector.

Abstract: An orthopaedic implant fixation using a surgically created bone cavity as a mold for forming an anchor from an in-situ hardenable material. An in-situ formed anchor of the present invention is especially useful for attaching an implant to osteoporotic cancellous bone. The injectable nature of the in-situ formed anchor allows implants to be adapted to minimally invasive surgical techniques. The present invention can be adapted to numerous implants or implant system components to include fasteners, pins, nails, intramedullary nails, and suture anchors. Applications include bone fracture fixation, bone fracture prevention, and soft-tissue repair.

Abstract: An orthopaedic implant fixation using a surgically created bone cavity as a mold for forming an anchor from an in-situ hardenable material. An in-situ formed anchor of the present invention is especially useful for attaching an implant to osteoporotic cancellous bone. The injectable nature of the in-situ formed anchor allows implants to be adapted to minimally invasive surgical techniques. The present invention can be adapted to numerous implants or implant system components to include fasteners, pins, nails, intramedullary nails, and suture anchors. Applications include bone fracture fixation, bone fracture prevention, and soft-tissue repair.

Abstract: A bone plate for use in anterior lumbar spinal fixation has interlocking components to prevent dislodgement of the plate due to anatomical forces. The exposed surface of the plate is smooth to prevent trauma to internal body tissue. The plate spans the intervertebral space with each end attached to an adjacent vertebrae by locking screws threadably engaged with tubular bone anchors. The bone anchors are threaded into the vertebrae and have a reduced diameter leading end which the locking screws expand to lock the anchor in the vertebrae and secure the end of the locking screw in the anchor. The plate has a countersunk cavity including portions overlapping the locking screws. A locking cap fits in the cavity to secure the other end of the locking screws from backing-out of the plate.

Abstract: An improved distraction bone screw and a method for its use are described. The distraction screw is comprised of an implantable distal segment and a detachably secured proximal segment. The distal segment includes a head portion and a threaded shank portion. The proximal segment is represented as an elongated body having an internal bore that extends through its length. A deployable member is disposed within the bore, which is extendible outside the internal bore to securely couple to the distal segment. As an assembly, the distraction screw is used to affix and realign bone during surgical reconstruction. Upon completion of the surgical work, the proximal segment is removed and the distal segment is left attached to the reconstructed bone. Securely affixed, the distal segment provides an additional point of fixation for the skeletal plates that are used to preserve the bony alignment while bone healing occurs.

Abstract: A stem-like bone fixation device allows for bony in-growth on its surface and across fracture fragments or between bones that are to be fused.