Abstract: A surgical instrument system comprising a handle and a shaft assembly is disclosed. The shaft assembly comprises an end effector, a release actuator, and a latch. The release actuator comprises a lock engaged with the handle when the release actuator is in a proximal position and disengaged from the handle when the release actuator is in a distal position. The latch is operably engaged with the release actuator and movable between a first position and a second position. The release actuator is configured to rotate the latch from the first position to the second position when the release actuator is moved toward the distal position. The latch comprises a catch configured to engage the handle when the latch is moved toward the second position. The catch is disengaged from the handle upon an additional manipulation of the release actuator. The additional manipulation is in a proximal direction.

Abstract: A surgical instrument includes a stapling head assembly, an anvil, an anvil adjustment assembly, and an indicator assembly. The anvil is configured to couple with the stapling head assembly. The anvil adjustment assembly includes a translating member, which is operable to translate relative to the body to thereby adjust a gap distance between the anvil and a distal surface of the stapling head assembly. The indicator assembly includes a first member and a second member. The first member is configured to translate in response to translation of the translating member relative to the body. The second member is configured to remain stationary relative to the body. The indicator assembly is configured to provide feedback indicating whether the gap distance is sized to release tissue from between the anvil and the distal surface based on positioning of the first member in relation to the second member.

Abstract: According to an aspect of the present disclosure, an endoscopic surgical device is provided. The surgical device includes a handle assembly including a drive mechanism actuatable by a trigger; and an endoscopic assembly including a proximal end portion extending from the handle assembly; a distal end portion pivotably connected to the proximal end portion of the endoscopic assembly; and a rotatable inner actuation shaft extending from the handle assembly and into the distal end portion of the endoscopic assembly, the inner actuation shaft including a flexible portion extending across the pivot connection. The surgical device includes an end effector selectively connectable to the distal end portion of the endoscopic assembly and to a distal portion of the rotatable inner actuation shaft. The end effector includes a splined inner tube rotatably supported in an outer tube; and a plurality of surgical anchors loaded in the inner tube of the end effector.

Abstract: The present invention is directed to devices for inserting bone staples into segments of bone. More specifically, embodiments of the present invention are adapted for accurately, selectively and simply providing for decompression of compression staples through application of a decompression force thereon, for placement of the legs of the decompressed compression staple in provided leg holes in adjacent bone segments while the compression staple remain decompressed, and for selective removal of the decompression force. In this respect, a staple inserter configured in accordance with an embodiment of the present invention is beneficial and useful in surgical procedure requiring bone tissue to join or rejoin with adjacent bone segments.

Abstract: Adjunct materials for delivery to colon tissue are provided. In general, the adjunct materials can be configured to be delivered to colon tissue by deployment of staples from a cartridge body of a surgical stapler to form at least one line of deployed staples. The adjunct material can be formed of a fiber matrix and include an effective amount of one or more medicants for delivery to the colon tissue. The medicant is disposed within and releasable from the adjunct material, and effective to encourage a desired effect on blood vessels, such as angiogenesis and/or vasodilation, along the at least one line of deployed staples. Methods of using a staple cartridge assembly or an end effector to apply such adjunct materials to colon tissue are also provided.

Abstract: Adjunct material to provide drug elution is a variety of different temporal and/or spatial patterns is provided. In general, a biocompatible adjunct having a plurality of distinct regions is configured to be delivered to tissue by deployment of staples in a cartridge body of a surgical stapler. Each of the distinct regions can be disposed at a different location on the adjunct material and can have a different adjunct construction. At least two of the regions releasably retain at least one medicant and each of the at least one medicants is releasable from one of the regions in a non-homogeneous manner with respect to at least one of time of release and location of release.

Abstract: A powered endoscopic surgical apparatus is provided and includes a handle including a housing, a power source supported in the housing; an endoscopic portion extending distally from the housing of the handle; an end effector assembly coupled to a distal end of the endoscopic portion, the end effector assembly including a pair of jaws configured to perform a surgical function; a driving member; a drive source including a motor powered by the power source and connected to the driving member; and a gear assembly engaged with the motor. The gear assembly including a gear rack provided on the driving member; and a main gear operatively connected with the gear rack, the motor spinning the main gear such that rotary motion of the main gear moves the driving member in an axial direction such that the driving member actuates the end effector to perform the surgical function.

Abstract: The invention provides improved devices, systems, and methods for tissue approximation and repair at treatment sites. The invention provides devices, systems, and methods that may more successfully approximate and repair tissue by improving the capture of tissue into the devices. The invention may be a one-way mechanism that allows tissue to enter the mechanism but not easily exit, such as a leaf-spring, a protrusion, a pivoting arm and one or more frictional elements.

Abstract: Various embodiments are directed to battery packs for use with surgical instruments. The battery packs may comprise a plurality of cells and at least a portion of the plurality of cells may not be electrically connected to one another. The battery packs may comprise a switch or other mechanism for interconnecting the plurality of cells and may also comprise, or be used in conjunction with, a discharge switch or plug configured to electrically connect an anode of the battery pack to a cathode of the battery pack, for example, via a resistive element.

Abstract: A staple cartridge assembly is disclosed. The staple cartridge assembly comprises staples including a base, staple legs extending from the base, and a platform extending laterally from the base. The staple cartridge assembly further comprises an implantable layer. The platforms of the staples are configured to support the implantable layer when the staples are implanted into the tissue of a patient. Staples are also disclosed which included an implantable adjunct positioned over the platform of the staple. The implantable adjuncts can include one or more compressible pockets. One or more medicaments can be positioned in the compressible pockets.

Abstract: A delivery system for an implantable vaso-occluding device. A non-planar heating chamber is disposed proximate to a distal end of an advancing member. Protruding from an interior surface of the non-planar heating chamber is a detachment fiber made from a polymeric material and having a closed distal end. At least one heating element is disposed on the interior surface of the non-planar heating chamber to produce sufficient heat to sever the detachment fiber. An articulation point is established between the vaso-occluding device and the delivery system. The vaso-occluding device remains at all times substantially self-centered while being advanced.

Abstract: A microcatheter for delivery of embolic fluids includes an outer member dimensioned for insertion within a blood vessel adjacent an embolization site. The outer member defines a first longitudinal lumen, and an inner member is selectively positionable within the first longitudinal lumen of the outer member. The inner member defines a second longitudinal lumen and has a delivery port in fluid communication with the second longitudinal lumen for passage and delivery of embolic fluids toward the embolization site. A valve is disposed within the outer member. The valve is dimensioned to establish a substantial seal about the inner member, to minimize entry of the embolic fluids within the first longitudinal lumen of the outer member subsequent to delivery thereof toward the embolization site.

Abstract: A device for enhancing the breathing efficiency of a patient is provided. The implantable device may include a deployed configuration with one or more helical sections with proximal end in a stand-off proximal end configuration. The stand-off proximal end configuration may reduce migration of the deployed device and may preserve implant tissue compression. Alternative configurations may include two or more helical sections with a transition section disposed between the two or more helical sections. A device may include a right-handed helical section and a left-handed helical section and the transition section comprises a switchback transition section. The switchback section may provide greater control of the device during deployment by limiting recoiling forces of a device comprising a spring material. The deployed device may compress the lung to increase a gas filling resistance of the compressed portion of the lung, and/or increase tension and elastic recoil in other portions of the lung.

Abstract: Elongate implant structures can be introduced into an airway system to a target airway axial region, often to apply lateral bending and/or compression forces against the lung tissue from within the airways for an extended period of time. Structures or features of the implants may inhibit tissue reactions that might otherwise allow portions of the device to eventually traverse through the wall of the airway. The devices may enhance the area bearing laterally on the tissue of a surrounding airway lumen wall. Embodiments may have features which increase the device friction with the airway to allow the device to grip the surrounding airway as the device is deployed. An appropriate adhesive may be introduced around the device in the lung. Hydrophilic material may inhibit biofilm formation, or features which induce some tissue ingrowth (stimulation of tissue growth) may enhance implanted device supported.

Abstract: One disclosed embodiment comprises a method for treating lesions in the carotid artery of a mammalian body. The method comprises transcervical access and blocking of blood flow through the common carotid artery (with or without blocking of blood flow through the external carotid artery), shunting blood from the internal carotid artery and treating the lesion in the carotid artery.

Abstract: An intraluminal occluding catheter and method for preventing the loss of gas insufflation from a physiological lumen during a medical procedure is presented. The intraluminal occluding catheter is generally comprised of a catheter shaft having a flexible balloon affixed on a distal intraluminal end and a plurality of independent channels extending through the catheter shaft from the external proximal end to the distal intraluminal end. Once inserted into a physiological lumen such as the bowel, the intraluminal occluding catheter controls the loss of insufflation proximally thereby improving the safety and efficiency of TAMIS as well as allowing for more controlled gas exchange to clear smoke or vapor.

Abstract: A posterior stabilized cruciate notch femoral cut guide shaped to fit over the distal end of a femur and including various cut guides to prepare the femur for a knee implant and methods for its use. Also described is a method for manufacturing the posterior stabilized cruciate notch femoral cut guide and various other cut guides and trialing instruments.

Abstract: An alignment guide includes a main body sized and shaped to contact the proximal end of a tibia, and a retaining guide coupled to the main body. The retaining guide includes guide surfaces and is adjustable relative to the main body such that an operator can intra-operatively adjust the position of the guide surfaces relative to the main body to capture the anterior and posterior cruciate ligament between the guide surfaces.

Abstract: The present invention in some embodiments thereof, relates to bone material removal devices (2100), for example, devices which change effective diameter. In some embodiments, a bone removal device comprises an expandable portion. In some embodiments, the expandable portion comprises one or more bone removing elements such as cutting teeth (2106). In some embodiments, a cutting tooth is movable between an open position, in which it is configured to widen a bore in a bone, and a closed position. In some embodiments, a cutting tooth of the bone removal device is formed with a curved, such as convex, cutting face (2114).

Abstract: An instrumentation system that includes a reamer sleeve having a reamer wall and a wedge body, the reamer wall being oriented about a central longitudinal axis. The reamer wall includes an inner passage that is sized to receive insertion of a reference instrument that is structured for placement in a canal in a bone. The inner passage can be centrally oriented about a longitudinal axis that is offset from at least the central longitudinal axis of the reamer wall. The wedge body can have a wedge surface that extends axially in a direction that is non-parallel and non-perpendicular to the central longitudinal axis. The apparatus also can include a cap having an opening that is sized to receive insertion of the wedge body. The cap can further include an inner wall having a tapered wall section that is oriented to matingly engage the wedge surface of the wedge body.

Abstract: A device (10) for use in orthopedic surgery includes a metallic central member (30). The device also includes an outer portion (20) comprising a polymer, which can be molded around the metallic central member. The outer portion thus surrounds the metallic central member. The outer portion has a profiled outer surface (40), such as teeth, ribs or ridges for removing bone. Engagement features for resisting relative movement between the metallic central member and the outer portion can comprise ridges, grooves (34, 36) and apertures (32) of the metallic central member, filled with polymer. The device can be a broach or rasp. A surgical instrument kit includes a plurality of differently sized devices of the kind described herein.

Abstract: Described herein include embodiments of devices, systems and methods for measuring drill depth, such as drill depths in bone material. For example, embodiments of drill depth measuring systems and associated methods are described. Some drill depth measuring systems can utilize at least resistance, capacitance, optical and/or acoustic sensing features for assisting the drill depth measuring system with determining drill depths and types of tissue being drilled into. Various other related features, devices and methods are also described.

Abstract: When an acetabular cup used in hip replacement surgery is to be affixed to the acetabulum using screws, the drill guide instruments of the invention are used to position a drill bit so that the screw holes drilled in the acetabulum are properly placed for optimum implantation of the acetabular cup. The drill guide is locked into the acetabular cup by spring loaded pins which position the guide over holes in the cup which accommodate the screws. The guide is used to position the drill bits and allow drilling. After drilling the guide is removed.

Abstract: This preparation set comprises a drill guide (31) comprising a bearing surface (33) intended to bear against a glenoid cavity, a passage orifice (35) intended for the passage of a guide pin (36) implanted in the glenoid cavity, and first and second guide orifices (37, 38) each opening into the bearing surface (33) and each intended to guide a drill bit (38) capable of realizing a bone bore in the glenoid cavity, the first and second guide orifices (37, 38) being inclined with respect to the extension axis of the passage orifice (35) and converging in the direction of the bearing surface (33); and a compactor (42) comprising a compaction portion (45) having a generally trapezoidal shape and intended to be impacted against the glenoid cavity so as to form a bone housing in the glenoid cavity, the compactor (42) further including a passage hole (49) extending at least partially in the compaction portion (45) and intended for the passage of the guide pin (36) implanted in the glenoid cavity.

Abstract: An aspiration thrombectomy catheter system includes an aspirator and an aspiration catheter for insertion in a blood vessel. The catheter has a shaft with a proximal end for connection with the aspirator and a tapering distal end with a tip for insertion in the vessel. A plurality of aspiration ports are arranged in sets along the tapering distal end, for aspirating thrombus from the vessel. At least one aspiration lumens within the shaft conducts thrombus from the vessel, through the aspiration ports, to the aspirator. Variably sized or shaped ports provide differing aspiration vectors for enhanced thrombus removal. The aspiration thrombectomy catheter additionally provides for uniform drug dispersion at a thrombotic area, alone or in combination with aspiration of the thrombus. In the event of an adverse reaction, drug dosage may be easily reduced by aspirating dispersed drugs back into the catheter.

Abstract: In one embodiment of the present invention, a method of applying ultrasonic energy to a treatment site within a patient's vasculature comprises positioning an ultrasound radiating member at a treatment site within a patient's vasculature. The method further comprises activating the ultrasound radiating member to produce pulses of ultrasonic energy at a cycle period T?1 second. The acoustic parameters such as peak power, pulse width, pulse repetition frequency and frequency or any combination of them can be varied non-linearly.

Abstract: A device for removing an obstruction from a lumen in a human or animal subject may include an inflatable balloon. The inflatable balloon may include a proximal tapered portion having a proximal taper angle, a central portion, and a distal tapered portion having a distal taper angle that is greater than the proximal taper angle. The balloon may also include at least one eversion feature on the proximal tapered portion and/or the distal tapered portion. The eversion feature may facilitate preferential eversion of the distal tapered portion into an inside of the balloon without the proximal tapered portion collapsing. Preferential eversion of the distal tapered portion may be provided by the differences in the distal and proximal taper angles and by one or more of a number of different types of eversion features.

Abstract: A surgical snare is provided having an operating wire and an outer sheath having a lumen extending therethrough, wherein the operating wire is disposed within the lumen and is longitudinally movable within the lumen. The surgical snare also has a first locking member attached to the operating wire and a second locking member attached to the outer sheath. The first locking member is frictionally engageable with the second locking member by sliding the outer sheath longitudinally along the operating wire until the first locking member contacts the second locking member. The operating wire is prevented from moving longitudinally with respect to the outer sheath when the first locking member is frictionally engaged with the second locking member.

Abstract: Deflectable guide catheters and methods, including methods for using defectable guide catheters to perform transnasal procedures within the ear, nose, throat, paranasal sinuses or cranium. Some deflectable guide catheters of the present invention comprise a substantially rigid tube, a helical spring attached to and extending from the distal end of the substantially rigid tube, a tubular plastic inner jacket, an outer plastic jacket substantially covering at least the helical spring member. The spring member is deflectable to cause the distal portion of the guide catheter to deflect to a curved configuration. In embodiments for transnasal use the deflectable guide catheter may have a length of less than 25 cm.

Abstract: A tongue cleaning device includes a tool head defining a trough that delivers the vacuum flow from an inlet to the inner surface disposed above a working edge for efficient removal of debris. The trough has a defined rear wall giving it a defined width. This allows the vacuum flow to be directed to where it is needed to remove debris. One configuration of the device has a head that defines a liquid distribution channel with an outlet disposed in front of the working edge with a supply of liquid being removably in fluid communication with the liquid distribution channel. The liquid supply being a bulk supply or a hand held bottle with a supply tube extending down the handle of the device. Another configuration of the device includes vacuum control openings controlled by the user's finger.

Abstract: Forceps include a tubular shaft, an inserted member, a gripping portion, a handle, and a fixing portion. The inserted member is a rod-like member that is inserted inside the tubular shaft and is movable in an axial direction inside the tubular shaft. The gripping portion is provided at a distal end of the inserted member and is coupled to a distal end of the tubular shaft. The handle is coupled to a terminal end of the inserted member. The fixing portion detachably fixes the handle to the tubular shaft in a state where the handle is coupled to the inserted member. The distal end of the tubular shaft has a larger diameter than the diameter of a main body of the tubular shaft. A joint portion, having a smaller diameter than the diameter of the main body of the tubular shaft, is formed at the terminal end of the inserted member. The handle is provided with a joint receptacle that houses the joint portion and is advanced and retracted by manipulation of the handle.

Abstract: The bifurcated forceps include a first pair of forceps having a first pair of opposed forceps or pincer arms and a second pair of opposed forceps or pincer arms. Each arm has a pivot end and a gripping end. Each pair is coupled at the pivot end and resiliently biased to a spaced apart position at the gripping end so that each pair may be independently pinched together, defining a gripping plane. The pivot ends of the two pairs are rotatable about a common pivot axis in a plane normal to the gripping planes, the arms in each pair being constrained to rotate to an identical radial angle in order to grip the same object at spaced apart positions. Adjacent arms in different pairs may have a mating blade and receptacle configuration to releasably lock the arms together to use the two pairs as a single pair.

Abstract: In the context of bone surgery and in particular arthroscopic surgery, there is frequently a need for the application of “percussive force” to the distal end component(s) of a surgical device, i.e., repetitive percutient or striking force analogous to that of a hammer driving a nail. Disclosed herein are mechanisms and methods for automating and/or controlling the application of such a percussive force so as to avoid the present need in the art for a “third hand”. The present invention addresses the significant and long felt need by providing a powered percussive driver device that may be controlled directly by the primary surgeon.

Abstract: A treatment method which treats a living tissue using an ultrasonic device includes making the ultrasonic device come in contact with the living tissue in a state where the product of a pressing force of the ultrasonic device to the living tissue, an amplitude of an ultrasonic vibration caused by the ultrasonic device, and a resonance frequency of the ultrasonic device becomes a predetermined value, and excising the living tissue in a state where the ultrasonic device is in contact with the living tissue.

Abstract: A device and method for visualization of the intravascular creation of autologous valves, and particularly venous valve, is disclosed herein. One aspect of the present technology, for example, is directed toward a delivery catheter that can include a lumen configured to receive a dissection assembly and a trough having a plurality of transducers electrically coupled to a proximal portion of the delivery catheter. At least one of the transducers can be configured to emit a signal towards a portion of a blood vessel adjacent the trough, and at least one of the transducers can be configured to receive a reflection of the emitted signal.

Abstract: Disclosed is an aortic punch comprising a first body member having a proximal end and a distal end, a second body member disposed at least partially within said first body member, a manual actuator, a piston having an anvil disposed at a distal end thereof, and a shear, said shear being integral with said second body member. The first body member and second body member are axially movable relative to one another between a fully extended position and a fully retracted position and within a range of intermediate positions while maintaining the piston and shear in position relative to each other in the axial direction, and separately the shear is axially movable via manual actuation relative to said anvil between an insertion position and a shearing position and a range of intermediate positions.

Abstract: Methods of providing sympathetic nerve blocks comprise inserting a portion of a catheter into a subject. A distal end of the catheter is positioned on a lateral side of at least one vertebra of a vertebral column of the subject proximate to a portion of a sympathetic nervous system of the subject. A medication is supplied through the catheter to effect a sympathetic nerve block in the subject. Methods of alleviating pain in lower extremities of subjects comprise inserting a portion of a catheter into a subject and supplying a medication through the catheter. Catheters and catheter assemblies may be used in administering such sympathetic nerve blocks. Catheters and catheter assemblies may be used in administering medication to one or more of a peripheral nervous system of a subject and a spinal cord of a subject.

Abstract: A biopsy needle assembly includes a mandrel within a cannula, the needle assembly is fired into a target tissue to obtain a tissue sample using a force source imparting movement to the needle assembly. The mandrel and cannula design, and force source characteristics minimize needle deflection, and allow the needle assembly to excise extended length tissue samples. The mandrel forms tissue retention ridges within a tissue sample region to reduce fragmentation of the tissue sample.

Abstract: A mounting structure for connecting a device to an organ. The mounting structure includes a mounting element defining a bore. The mounting element is adapted for mounting to an exterior surface of the organ of a living subject. The mounting element includes a collar having a deformable wall defining a main bore. A gimbal ring disposed within the main bore and within the collar is included, the gimbal ring defining a gimbal bore co-axial with the main bore and including a plurality of separate arcuate elements cooperatively disposed in a circumferential direction around the gimbal bore, the plurality of separate arcuate elements being movable toward one another to constrict the gimbal bore.

Abstract: A trocar set includes a handle portion, a first sleeve, a second sleeve, and a gasbag. The handle portion includes a grip, a connection part, and a first gas valve. The connection part extends from the grip and includes an assembling channel. The first gas valve is connected to the connection part and communicates with the assembling channel. An assembling end of the first sleeve is assembled to the connection portion. A sleeving end of the first sleeve is provided with a first opening. The second sleeve is retractably connected to the sleeving end of the first sleeve. A sleeve wall of the second sleeve is provided with a second opening. The gasbag is connected to an end of the second sleeve away from the sleeving end and corresponds to the second opening. The design of the retractable sleeves is benefit to perform operation.

Abstract: A catheter system for retrieving a leadless cardiac pacemaker from a patient is provided. The cardiac pacemaker can include a docking or retrieval feature configured to be grasped by the catheter system. In some embodiments, the retrieval catheter can include a snare configured to engage the retrieval feature of the pacemaker. The retrieval catheter can include a torque shaft selectively connectable to a docking cap and be configured to apply rotational torque to a pacemaker to be retrieved. Methods of delivering the leadless cardiac pacemaker with the delivery system are also provided.

Abstract: An embryo transfer catheter (10) is described comprising an outer catheter body (12) having first and second lumens (14, 16). The second lumen (16) is adapted to receive an internal catheter (not shown) with a single lumen which, in use, will allow passage of an embryo or embryo-containing cannula (not shown) into the uterus (18) of the recipient. An inflatable balloon (20) is provided at a distal end of the first lumen (14). The inflatable balloon (20) is designed to be as small as possible in its inflated condition while still being retained in the uterus (18). The shape of the balloon (20) is adapted in its inflated state to conform to just the lowest part of the uterus (18). The aim in designing the balloon (20) as small as possible is to leave as much endometrium accessible to the embryo for implantation as possible, and to occupy as little volume as possible within the uterine cavity and to exert as little pressure as possible to avoid causing contractions, while still being retained in the uterus (18).

Abstract: A spinal construct is provided including a first fastener, a second fastener and a connector. Each fastener includes a first end and a second end configured for penetrating tissue. The connector has two ends. Each end of the connector includes an expandable member. The first end of each fastener is engageable to an expandable member of the connector to fix the fastener to the connector. The first and second ends of the connector are connected by a bridge. The spinal construct also includes securing members for attaching the connector to the fasteners. A method for treating a spinal disorder with the spinal construct is also provided.

Abstract: A subcutaneous implantable device for aligning a spine having a plurality of vertebrae, including a stabilizing plate assembly, a first rod, including a first end, and a second end coupled to the stabilizing plate assembly, a second rod, including a third end, and a fourth end coupled to the stabilizing plate assembly, a winding assembly, and a tensioning member including a line, the line having a first end, and a second end secured to the winding assembly, wherein the line is connected to the stabilizing plate assembly.

Abstract: A vertebral fixing system having a flexible elongated member, a connecting part, and an anchor, where the anchor may engage a bone structure (e.g., a vertebra) through an opening of the connecting part and the flexible elongated member may connect to the connecting part. In some cases, the vertebral fixing system may include a tightening part configured to apply a tension to the elongated member and/or secure the elongated member with respect to the connecting part. The vertebral fixing system may be configured to receive a rod and may be capable of connecting thereto. The connecting part may have a plurality of connecting members, where at least one of the connecting members includes an opening for receiving the anchor and at least one of the connecting members connects to the elongated member.

Abstract: A discontinuously double-threaded bone screw includes a drive head and anchoring body consisting of a cylindro-conical core over which extend at least two cylindro-conical threads, the anchoring body including anchoring portions of different profiles, ensuring an anchoring corresponding to different bone hardnesses and strengths, the anchoring body including, below the drive head, a first anchoring portion with a conical core and two threads with cylindrical profile and identical pitch, a second anchoring portion with a cylindrical core and a single cylindrical thread over ¼ turn, a third anchoring portion with a cylindrical core and two threads with cylindrical profile over ½ turn, a fourth anchoring portion including a cylindrical core and a single thread with cylindrical profile n turn based on total length of the bone screw, and a fifth anchoring portion including a conical core and two threads with conical profile forming the tip of the bone screw.

Abstract: A double-headed pedicle screw is provided. The double-headed pedicle screw includes a threaded shaft portion and a plurality of yoke assemblies supported by the threaded shaft portion. Each of the yoke assemblies includes a recess configured to receive a portion of a rod, alignment structure, or immobilization structure therein. Each of the yoke assemblies is configured for pivoting movement relative to the threaded shaft portion independent of the pivoting movement of the other yoke assemblies.

Abstract: A receiver subassembly adapted to couple with a universal shank to form a bone anchor assembly. The universal shank having an integral upper capture structure with opposed spaced apart flat side surfaces. The receiver subassembly including a receiver including a distal opening for bottom loading of the capture structure of the universal shank there-through. The receiver supporting a retainer and a positioner within the receiver. The positioner supporting a position of the retainer within the receiver. The retainer configured to couple with the capture structure when the capture structure extends at least partially through the distal opening.

Abstract: Anterior cervical plates for spinal surgery employing anchor backout prevention devices, and related systems and methods are disclosed. A spinal column includes vertebrae in an articulating structure. Medical intervention may involve limiting the relative motion between vertebrae by fusing at least first and second vertebrae together with osteosynthesis systems. The systems include a plate attached to anterior surfaces of the first and second vertebrae with anchors extending through passageways in the plate. By including one or more anchor backout prevention devices to the plate, movements causing the anchors to disengage from the vertebrae may be avoided. The devices may include a positioning guide, and locking magnets. The implementation of a combination of these devices into the plate may provide greater robustness against failure than any of the devices individually. In this manner, the useful life of the plate within a patient may be lengthened.

Abstract: This invention relates to an improved structure for an interspinous stabilization device that more evenly distributes loads throughout the adjacent vertebrae than known interspinous stabilization devices, and further readily compensates for graft settling so as to maintain continued axial loading of the graft. More specifically, this invention relates to a medical device that helps in performing a spinal fusion procedure by holding the bone graft in place and stabilizing the facet screw by a plate that is attached to it. The invention also performs a dynamic function that compensates for settling of the bone graft over time. This dynamic function may, if desired, be enhanced by a movement-limiting mechanism that allows extension but not flexion such that the bone graft fusion remains in contact and fusion takes place.