Abstract: The present invention relates to alignment systems and methods for detecting a distal hole of an intramedullary nail. A jig is attached to the proximal end of the nail and also mounted on the bone. The jig has an adjustable positioning head that includes a drill axis hole along with an alignment pin. The alignment pin includes reference marks that are visible in X-ray images and helps to align the positioning head drill axis with the distal hole of the intramedullary nail. A light source is insertable into the nail in order to shine light out of the distal hole to illuminate a spot on the bone surface as an alignment aid. Viewing optics are mountable on the positioning head for viewing the illuminated spot created by the light source in the intramedullary nail.

Abstract: A bone cutting assembly includes a guide pin that may be securely inserted into a bone to define a cutting axis. The bone cutting assembly also includes a housing having a cam surface and features for temporarily fastening the housing to the bone. The bone cutting assembly also includes a burr mounting arm that rotatably and slidably fits onto the guide pin so that the arm can swing around the cutting axis and also translate up and down the guide pin. A user may move the burr mounting arm about the cutting axis so that the arm follows along the cam surface of the housing.

Abstract: A medical instrument includes a base; an upper member; and a linkage mechanism coupled to the base and the upper member and being operable to maintain the upper member in a variable fixed position that is substantially parallel to the base and spaced a predetermined, variable distance therefrom, wherein the linkage mechanism includes at least three linkage elements that are arranged at angles relative to one another such that when one link element opens, the other link elements open with at an equal angle resulting in the upper member being constrained to remain parallel to the base.

Abstract: An adapter attached between a syringe containing a bone void filler and the head of a cannulated surgical screw allows the cannulated surgical screw to be used as a port to inject bone void filler into a bone void during the course of a surgical repair which would use a surgical screw to attach broken or separated bone fragments providing a more secure bone anchor matrix within which the surgical screw is set.

Abstract: Instruments, implants and methods are provided for positioning spinal implants in a spinal disc space between adjacent vertebrae. The instruments provide a low profile engagement with the implants and facilitate insertion while minimizing tissue retraction and exposure of the tissue and neural elements to the instrumentation in the approach to the disc space.

Abstract: Methods for predetermining a contour of a resected bone surface and assessing a fit of a prosthesis on the resected bone surface, for designing prostheses to fit discrete patient populations, and for designing customized prostheses.

Abstract: A polyaxial screwdriver for inserting a bone screw in a vertebra. A polyaxial bone screw assembly includes a coupling element. When a screw engaging end of the polyaxial screwdriver is lowered on the head of the bone screw, the complimentary surfaces of the screw engaging end of the screwdriver and the head of the screw self-align. A ratchet mechanism formed in the screwdriver provides progressive and automatic locking of the polyaxial screwdriver to the coupling element and prevents the accidental unthreading from the coupling element. In another embodiment of the polyaxial screwdriver, a collet slides over the outside surface of the upper end of the coupling element and locks on to the coupling element. In yet another embodiment of a polyaxial screwdriver, the outer sleeve of the polyaxial screwdriver has a split end that securely engages the coupling element.

Abstract: A surgical instrument for securing an anchor in a target area of the skull of a patient, wherein the anchor has a shaped surface, a top and a base. In one embodiment, the surgical instrument includes a driver having a first end, an opposite, second end, and a body portion defined therebetween forming a bore therein along a longitudinal axis, where the bore is configured to allow the anchor to be received therein, a first inner surface formed inside the bore proximate to the first end, wherein the first inner surface is formed with a shape that is complimentary to the shaped surface of the anchor, and a second inner surface formed inside the bore and between the first inner surface and the second end, wherein the second inner surface is formed with a shape that is different from that of the first inner surface.

Abstract: The present invention is a surgical tool for implanting an electrode array and its connected cable within an orbital socket. The insertion tool is used to aid the surgeon in pulling the electrode wire and array through the scull, four-rectus muscles of the eye, and the sclera. The insertion tool consists of a medical grade ABS material that is commonly used in various medical products.

Abstract: In one implementation, a method is disclosed in which a lock sensing mode is entered for a robotic surgical instrument. In the lock sensing mode, the degrees of freedom of movement in the robotic surgical instrument are switchably reduced. Further in the lock sensing mode, one or more end effectors of the robotic surgical instrument are switchably clamped together in the robotic surgical instrument. An increased level of torque may also be applied to the end effectors to increase a gripping force applied by the one or more end effectors in response to the reduced degrees of freedom of movement in the robotic surgical instrument.

Abstract: Systems and methods introduce and deploy prosthesis into a blood vessel or hollow body organ by intra-vascular access. The prosthesis is secured in place by fasteners which are implanted by an applier that is also deployed by intra-vascular access. The applier is configured to permit controlled, selective release of the fastener in a step that is independent of the step of implantation.

Abstract: A suture instrument includes: a therapeutic insertion section having a suture section for suturing tissue; a cylindrical main operation unit; a rod section in the main operation unit, for discharging a suture thread and end section members connected to the suture thread; a pusher's distal end section for pressing the end section member; and a guide mechanism for rotating the rod section after linear movement of the pusher's distal end section at a position where one of the end section member is fed from a distal end of the suture section, the rod section being rotated in the circumferential direction to a position where the other one of the end section members is fed from the distal end of the suture section, so that each one of the end section members is discharged one after another and so that the end section members can be separated finally.

Abstract: Methods and devices for partitioning or plicating a region of a hollow body organ are described herein. These methods and devices relate generally to medical apparatus and methods and more particularly to devices and methods for affecting a change in the function of a hollow body organ, particularly a stomach, intestine or gastrointestinal tract. These changes can include reducing the volume capacity of the hollow body organ, disrupting or altering the normal function of the organ, functionally excluding certain sections of the organ either by affixing adjacent tissue or excising certain regions, or affecting or correcting the response of the organ to naturally occurring stimuli, such as ingestion.

Abstract: An intestinal anastomotic surgery aid 1 is constituted with a cylindrical portion 40 for covering the proximal end side of an engaging rod 28, and a cover portion 41 that extends from the cylindrical portion 40 towards the distal end side of the engaging rod 28. The proximal end part of the cylindrical portion 40 is inserted to a recessed portion 26 of a device main body 21 to be held to the device main body 21. The anus-side piece of the intestine is tied with a suture to be held to the outer face of the cylindrical portion 40.

Abstract: An apparatus and method for accurately making a limbal relaxing incision. An example universal limbal relaxing guide (ULRIG) includes an inner rotating ring, a measurement gauge, a base unit and bumpers. The inner rotating ring and measurement gauge rotate concentrically relative to the base unit. The inner ring guides a keratome along an arc of constant radius. The measurement gauge enables the user to select the length of the arc and the bumpers prevent the keratome from overshooting the desired incision length. Because the thin degree ring rotates relative to the base unit, the example ULRIG can be used with more than one style of keratome. Multiple marks on a pointing bumper enable the user to adjust the resultant incision length for the cornea size of an individual patient.

Abstract: A head portion includes an engaging portion capable of engaging with an engagement portion, a slit formed by cutting a part of a peripheral wall surface of the engaging portion, a protuberance which protrudes inward from the peripheral wall surface of the engaging portion, the protuberance including a slope the height of projection of which gradually increases along the circumference of the peripheral wall and which is oriented in a direction of rotation in a rotating operation, and a stop surface extending in radial directions of the engaging portion. The head portion includes an elastically deformable portion configured to cause at least one of two opposite side portions of the slit to be elastically deformed so that the slit is widened until a preset value is reached by the torque applied from the engaging portion to the engagement portion with the protuberance in mesh with an interlocking portion.

Abstract: The present invention relates to lancet device by which a lancet is displaceable along a piercing path to generate a piercing wound in a skin surface, in particular to obtain body fluid for diagnostic purposes. To achieve performance of a piercing movement which is low in noise and shock, the lancet drive may include a control unit for regulating the piercing depth of the lancet and the lancet may be implemented to oscillate freely out in the piercing direction without delimitation by a mechanical piercing depth stop.

Abstract: Devices and methods are disclosed for the control of blood perfusion pressure within a blood vessel that undergoes arterialization. A cannula is introduced that contains a stenosis that either resorbs or is removed in time, allowing a gradual increase in blood pressure between two blood passages connected at either ends of the cannula. Particular emphasis has been made with the use of the cannula for the vessels in the heart.

Abstract: The present invention relates generally to a catheter having a torque transmitting shaft which retains adequate flexibility. The catheter includes an elongate shaft having an outer surface. In a preferred embodiment, a raised pattern is disposed on the outer surface. Preferably, the raised pattern improves the transmission of torque along the elongate shaft by including a series of bearing points which contact other bearing points along the shaft when torqued.

Abstract: A device for treatment of nosebleeds having an elongated body configured to be positioned between the upper gum and the portion of the face below the nose and above the top lip of a human. When so positioned intra-orally, the device exerts pressure on an area of nasal vascularization of the human. Also, a nosebleed package having a sterile inside environment and a nosebleed device packaged therein, and a box containing a plurality of nosebleed packages.

Abstract: Retrievable blood clot filter devices implantable within a blood vessel, including methods and apparatuses for retrieving such devices, are disclosed. The retrievable blood clot filter device can include an apical head, and a plurality of elongated filter legs configured to expand between a collapsed position and an expanded position within the blood vessel. A bendable anchoring member disposed on one or more filter support members can be used to secure the blood clot filter device along the inner wall of the blood vessel. The anchoring members can be configured to bend and retract into a number of filter tubes slidably disposed along the support members, allowing the blood clot filter device to be removed with a retrieval apparatus.

Abstract: An improved embolic filter frame having looped support struts. The frame configuration provides enhanced longitudinal compliance, improved sealing against a vessel wall, low profile delivery, and a short deployed length. The looped support struts have a high degree of “radial” stiffness with a low degree of “longitudinal” stiffness. In the deployed state, the frame exerts a relatively high stress onto a vessel wall to maintain an effective seal, yet remains compliant in the longitudinal direction. Minor displacements of the support wire or catheter are therefore not translated to the filter. The looped support struts elongate when tensioned and assume a compressed and essentially linear form. While constrained in this linear state by a delivery catheter, the support struts exert minimal stress onto the delivery system. The overall delivery profile and stiffness are therefore reduced.

Abstract: A guided filter system for temporary placement of a filter in an artery or vein is disclosed. The system includes a guidewire slideable through a wire guide included in a distal region of a support wire. The support wire has an expandable filter, which is operable between a collapsed or enlarged condition. A variety of endovascular devices, including angioplasty, atherectomy, and stent-deployment catheters, are insertable over the guidewire and/or the support wire. Methods of using the guided filter system to direct and exchange endovascular devices to a region of interest, and to entrap and remove embolic material from the vessel are also disclosed.

Abstract: Embodiments of the invention include a medical instrument with a sealing device. In embodiments, the medical instrument is an endoscopic device having a seal between an elongate shaft member and/or on a portion of a handle to, for example, prevent flow communication between a lumen of the elongate member and the external environment.

Abstract: Systems and methods for soft tissue to bone repairs, without knot tying.

Abstract: Methods of attaching a soft tissue to an adjacent bone at a defect site are provided. At least one adjustable loop of a flexible construct is passed through the soft tissue. The at least one adjustable loop is passed through a passage construct. A locking member is passed through the at least one adjustable loop and the adjustable loop is reduced about or within the locking member such that the at least one loop is frictionally retained in the passage construct and locked in place by the locking member to thereby secure the soft tissue.

Abstract: Cephalad and caudal vertebral facet joint prostheses and methods of use are provided. The cephalad prostheses are adapted and configured to be attached to a lamina portion of a vertebra without blocking a pedicle portion of the cephalad vertebra. In some embodiments, the prosthesis is attached with a non-invasive support member, such as a clamp. In other embodiments, a translaminar screw may be used for additional fixation.

Abstract: An adjustable spine distraction implant alleviates pain associated with spinal stenosis and facet arthropathy by expanding the volume and/or cross sectional area in the spinal canal and/or neural foramen. The adjustable implant provides a spinal extension inhibitor. The implant includes elliptical or oval shaped adjustable member or spacer for positioning between and adjustably spacing apart the spinous processes.

Abstract: Devices and methods for spinal stabilization include first and second anchor assemblies engageable to respective ones of first and second vertebrae and a connecting element engageable to the first and second anchor assemblies. The connecting element includes opposite first and second end members and a bumper assembly between the end members that flexibly connects the end members so the connecting element can provide dynamic stabilization of the spinal column when engaged to the anchor assemblies.

Abstract: Introducer Device comprises (a) Housing including (1) Housing Lumen sized and shaped to slidably receive a visualization device therein and (2) Slot sized to receive therein a projection extending from visualization device received in Lumen radially away from Lumen; (b) Sheath extending distally from handle and being sized and shaped for insertion through a natural body opening into a hollow body organ, Sheath including a fluid delivery lumen delivering heated fluid to the organ and a fluid return lumen withdrawing the fluid after it has been circulated through the organ; (c) Connector including Connector Lumen aligned with Lumen and sized and shaped to slidably receive therein visualization device; (d) Locking arrangement movably coupled to Housing, movement relative to the housing opening and closing Slot; and (e) Adjustment mechanism moving Connector relative to Housing to adjust distance between a proximal end of Connector Lumen and a distal end of Sheath.

Abstract: A system for anchoring at least a portion of material to a vertebral body is disclosed. The anchoring system comprises a base configured to affix to the vertebral body and configured to receive the at least a portion of material, and an anchoring mechanism configured to engage with the base and configured to anchor the at least a portion of material, wherein the mechanism comprises at least one elastic element configured to apply pressure to the at least a portion of material so as to anchor the at least a portion of material to the base. Also, a method for attaching at least a portion of material to bone is disclosed.

Abstract: A spinal fixation element includes a screw and a washer. The screw comprises an elongated body of a first diameter and the body includes a threaded portion at a distal end and a semispherical head of a second diameter at a proximal end. The second diameter is larger than the first diameter. The washer comprises a semispherical through opening of a third diameter at the top, of a fourth diameter in the middle and of a fifth diameter at the bottom. The third diameter is slightly smaller than the second diameter, the fourth diameter is slightly larger than the second diameter and the fifth diameter is smaller than the second diameter. The washer surrounds the semispherical head, is non-removably attached to the semispherical head and is rotatable and positionable at an angle relative to the elongated body.

Abstract: Apparatus and methods for facet fusion include an insertion tool and a guide tool coupled to one another. The insertion tool has a proximal end portion and an opposite distal end portion. The distal end portion of the insertion tool is configured to retain an interbody implant, such as, for example, an inter-facet implant configured for placement between a superior facet and inferior facet of a facet joint. The proximal end portion of the insertion tool includes a handle. The guide tool includes an elongated body with a passage extending between and opening at its distal and proximal ends. A linking member extends between and adjustably connects the guide tool to the insertion tool so that the passage of the guide tool is alignable with the interbody implant retained on the insertion tool while the insertion tool and guide tool are in substantially orthogonal relation to one another.

Abstract: A system and a method for bone fixation are provided. A bone plate may be secured to at least one bone. A monolithic region of the bone plate may be bent to a bent configuration. A strut may be connected to the bone plate. In some embodiments, the strut may be connected at spaced positions of the bone plate that opposingly flank the monolithic region, such that the bent configuration is stabilized.

Abstract: The present invention relates to an orthopedic plate and screw system and instruments for surgical fixation of a small bone or bones including specifically the small bones of the spine. The plate facilitates three dimensional contouring to provide for a variety of applications and to accommodate individual variation in bone shape. The plate has a modified x shape including a central trunk portion including one or more screw holes along a longitudinal axis and a set of divergent upper and an oppositely extending set of divergent lower arms, each arm including screw holes which are placed at a radially equal distance but which diverging asymmetrically from the longitudinal axis relative to its paired upper or lower mate. The screws of the system are self-starting, self-tapping screws including the option of partial or full cannulation. In a further embodiment, the plate is intended for use through the length of the spine.

Abstract: Relatively non-invasive devices and methods for heating or cooling a patient's body are disclosed. Devices and methods for treating ischemic conditions by inducing therapeutic hypothermia are disclosed. Devices and methods for inducing therapeutic hypothermia through esophageal cooling are disclosed. Devices and methods for operative temperature management are disclosed.

Abstract: The present invention relates to devices and methods for the treatment of diseases in the vasculature, and more specifically, devices and methods for treatment of aneurysms found in blood vessels. In a first embodiment of the present invention, a two part prostheses, where one part is an expandable sponge structure and the other part is an expandable tubular mesh structure, is provided. In the first embodiment, the expandable sponge structure is intended to fill the aneurysm cavity to prevent further dilatation of the vessel wall by creating a buffer or barrier between the pressurized pulsating blood flow and the thinning vessel wall. In the first embodiment, the expandable tubular mesh structure is placed across the aneurysm, contacting the inner wall of healthy vessel proximal and distal to the aneurysm.

Abstract: The present invention relates to devices and methods for the treatment of diseases in the vasculature, and more specifically, devices and methods for treatment of aneurysms found in blood vessels. In a first embodiment of the present invention, a two part prostheses, where one part is an expandable sponge structure and the other part is an expandable tubular mesh structure, is provided. In the first embodiment, the expandable sponge structure is intended to fill the aneurysm cavity to prevent further dilatation of the vessel wall by creating a buffer or barrier between the pressurized pulsating blood flow and the thinning vessel wall. In the first embodiment, the expandable tubular mesh structure is placed across the aneurysm, contacting the inner wall of healthy vessel proximal and distal to the aneurysm.

Abstract: An apparatus for treating an area of bifurcation where a principal body conduit separates into at least two secondary conduits comprises a radially expandable first stent body. The first stent body has a substantially conical shape and a first end having a greater diameter than a second end when fully expanded. The first stent body is preferably shaped to be independent of any other stent bodies, and is free of any means for connecting to any other stent bodies when fully expanded.

Abstract: The invention relates to a stent (1) for introducing into human body cavities, in particular into blood vessels, comprising a proximal first end to be introduced (2) and a distal final end to be introduced (3), a sleeve-like stent body (4) made of biocompatible material, and at least one support wire (5) provided as a support body within the stent body (4), the support wire (5), when the stent is in the tensioned state, resting against the inside of the stent body (4) in the shape of a spiral and the stent body (4), when the stent is in a compressed state, being collapsed and expandable into a tensioned state. The proximal end of the support wire (5) in the region of the proximal first end to be introduced (2) is firmly attached to the stent body (4) and the distal end of the support wire, when the stent is in the compressed state, extending from the distal final end (3) of the stent body (4) to be introduced.

Abstract: A tether guided bifurcated stent having a generally tubular main body extending along a longitudinal axis connected to a side branch assembly. Both the main stent body and the side branch assembly are capable of forming an unexpanded configuration and an expanded configuration. The bifurcation's expansion is facilitated by a force exerted by the tether. When the side branch assembly is expanded it forms a secondary tubular region defining a generally tubular shape extending at an angle to the longitudinal axis of the main tubular body.

Abstract: A method for percutaneously replacing a heart valve of a patient. In some embodiments the method includes the steps of percutaneously delivering a replacement valve and an expandable anchor to a vicinity of the heart valve in an unexpanded configuration; expanding the anchor to a deployed configuration in which the anchor contacts tissue at a first anchor site; repositioning the anchor to a second anchor site; and deploying the anchor at the second anchor site.

Abstract: A mitral cerclage annuloplasty apparatus comprises a tissue protective device and a knot delivery device. The tissue protective device comprises a first protective tube and a second protective tube. The knot delivery device comprises a tube wherein a loose knot is looped around its distal end through a hole and wherein tight knot is formed when the distal end of the tube is cut open. Alternatively, the knot delivery device comprises an inner tube and outer tube. The inner tube is insertable and rotatable inside the outer tube. When the tubes are in a closed position by rotating either the outer tube or the inner tube, a hole is created near its distal end. When the tubes are in open position by rotating either the outer tube or the inner tube, the hole joins the opening of the outer tube and lengthens.

Abstract: A system for measuring the size of a capsular bag of an eye of a subject includes a size indicator and a sizing gauge. The size indicator is configured for insertion into a capsular bag and includes a peripheral portion and a pair of arms. The peripheral portion is configured to engage the capsular bag. Each of the arms has a proximal end and a distal end, the arms being joined to one another at the proximal ends. The peripheral portion is joined to the distal ends of the arms. The arms form an angle that depends on a size of the capsular bag into which the size indicator is placed. The sizing gauge has a body having a front surface, along with first and second features disposed along or behind the front surface. The features are configured to correspond to an angle that is within a predetermined range of angles of the arms of the size indicator when the size indicator is placed within a capsular bag.

Abstract: An improved multifocal design for an ocular implant is provided. This ocular implant includes an intraocular lens (IOL) and a number of haptics. The IOL passes optical energy. A microstructure within the IOL places the IOL under tension. The microstructure is operable to be broken in a controlled manner to release tension in the IOL and reshape the IOL. This may be done at any time post operatively and in conjunction with wavefront aberrometry to provide improved results. The haptics mechanically couple to the IOL in order to position and secure the IOL within the eye.

Abstract: A continuous loop and button construct and technique for ligament repair and fixation, including bone to bone, or soft tissue to bone. The continuous loop, which is attached to the button, is formed of a flexible material and is provided with at least one joined region (a bridged, stitched, bonded or knotted region) to form a closed loop figure-8 construct with proximal and distal openings with respect to the fixation device. The figure-8 construct (either bridged, stitched, bonded or knotted) is adapted for attachment to a bone block of a BTB graft, for example, and used for ligament reconstruction.

Abstract: A vertebral implant for fusing adjacent vertebrae or for replacing vertebral bodies is disclosed. The implant is a biocompatible metal, resorbable, or radiolucent implant conforming substantially in size and shape with an end plate of a vertebra. The implant preferably has a wedge-shaped profile to restore disc height and the natural curvature of the spine. The top and bottom surfaces of the implant have areas with a plurality of teeth to resist expulsion and provide initial stability and areas devoid of any protrusions to receive implantation instrumentation. The implant also has a stackability feature. The implant provides initial stability needed for fusion without stress shielding.

Abstract: A motion preserving implant having first and second bearing members and a biasing member disposed therebetween operable to provide resistance to the translation of the bodies with respect to one another. An intervertebral implant having first and second bearing members, a translatable member, a resilient connection between the translatable member and one of the bearing members to allow for relative motion therebetween and bearing surfaces of the translatable member and the other bearing member to allow complex, natural motion between the bearing members. A spinal implant having upper and lower bodies and an articulation surface that allows for polyaxial articulation and translation through a concave articulation surface having a first radius of curvature and a second radius of curvature in at least one plane, and a convex articulation surface having the first radius of curvature in the same plane.

Abstract: An artificial disc prosthesis is provided. The prosthesis enables spinal segment alignment by having a variable height across its surface. The variable height is achieved by an asymmetric artificial nucleus or by at least one variable height end plate. The prosthesis may have a central keel on one end plate and an offset pair of keels on a second end plate. The nucleus may engage a slot or trough in an inner surface of an end plate. The trough can be open on the posterior or anterior end to allow the nucleus to slide into the trough without undue distraction of adjacent vertebrae. The nucleus can be prevented from moving out of the trough by inserting a stop in the trough.

Abstract: Methods of treating a herniated disc are provided. In one embodiment, the method includes establishing a first biocompatible support member to, within, or posterior to a portion of an anulus adjacent a herniated segment of the anulus and establishing a second biocompatible support member to, within, or posterior to the anulus adjacent the segment or within an adjacent vertebral body. The method further includes connecting the first and second support members with a connection member and applying tension between the first and second support members along the connection member, thereby displacing the herniated segment.