Abstract: The invention provides a surgical apparatus for performing a controlled resection of the neck of a femur during a hip replacement procedure, the surgical apparatus comprising: a body portion. The body portion comprises a frame that is mountable on a femoral head of the femur to position the body portion with respect to a centre of the femoral head. The body portion also includes a resection guide for indicating a position of a resection plane on the femoral neck, and an arm extending from the frame and including markings for reading off a femoral head offset. The apparatus also includes a connector for mounting the body portion on an intramedullary rod located in an intramedullary canal of the femur, and for slidably receiving the arm. The connector includes a pointer. The femoral head offset is indicated by reading the position of the pointer relative to the markings on the arm.

Abstract: A surgical tool guide comprises an anchor body extending between a proximal end and a distal end along an anchor axis. The anchor body has a piercing element at the proximal end. An angle adjustor arcuately extends between two opposed ends. The angle adjustor is mounted to the anchor body between the proximal end and the distal end. A guide body is cannulated along a longitudinal length thereof to define a guide passage extending along a guide axis. The guide body is mounted to the angle adjustor such that the guide axis intersects the anchor axis at a target surgical point and an angle is defined between the anchor axis and the guide axis. The anchor body and/or the guide body is displaceable relative to the other along the angle adjustor to vary at least one of the angle and a depth of the target surgical point.

Abstract: A drill component is provided that enables determining the drill component's insertion depth into bone via direct measurements. The direct measurements help provide more consistently accurate insertion depth measurements as compared to typical insertion depth measurement methods that indirectly determine insertion depth using cannulas outside of the bone. The determined insertion depth corresponds to an implant size or length that a surgeon should select for a procedure. The drill component includes a shaft having an insertion end that includes multiple indications or markings that are visible on radiographic or fluoroscopic images. From one or more captured radiographic or fluoroscopic images of the drill component advanced into bone, a surgeon may count a quantity of indications or markings of the drill component on the one or more radiographic or fluoroscopic images to determine the drill component's insertion depth into the bone.

Abstract: Instruments and surgical techniques may be used to correct a bone deformity, such as a bunion in which a metatarsal is misaligned with respect to a medial cuneiform. In some examples, a bone cutting guide is utilized to cut an end of the metatarsal and/or an end of the medial cuneiform to facilitate realignment of the bones. The cutting guide can have a pivotable cut guide surface along which a cutting instrument is translated to provide a precise bone cut. In some applications, after suitably preparing and aligning the bones, the bones are compressed together using a fixation pin. The fixation pin can be driven through one of the bones, into the second bone, and then further driven to compress the bones together.

Abstract: Methods and systems disclosed herein provide systems and methods for anchor placement.

Abstract: A technique for correcting a bone deformity, such as a bunion, may be performed using an instrument. The technique may include preparing an end of a first metatarsal and preparing an end of a medial cuneiform opposing the end of the first metatarsal. The technique may also include moving the first metatarsal relative to the medial cuneiform. The technique can involve inserting the instrument between a first metatarsal and a second metatarsal.

Abstract: A hard tissue fixation staple-plate interlocking device can include a recess in a staple body or a plate. The device can also include a locking part of the other of the staple body or plate. The device can be reconfigurable between an insertion configuration and an interlocked configuration. In the insertion configuration, the locking part can slide into the recess in a translation sliding motion that is parallel to a sliding motion of the legs of the staple, as the legs of the staple slide through the holes in the plate. In the interlocked configuration, the locking part can be at least partially in the recess, and recess surface portions can engage part surface portions and inhibit movement of the staple and plate out of the interlocked configuration. Also, multiple staples and screws can be interlocked with the plate, with staples being at non-parallel angles to each other.

Abstract: A device includes an outer sleeve of flexible material forming an outer conduit extending longitudinally therethrough for the insertion of a bone treatment device (“BTD”) to target sites within a living body. A distal opening of the outer conduit is open so that, when the outer sleeve is in a desired position within the body, BTD is inserted through the outer conduit exits the outer sleeve adjacent to a target portion of a bone. The device also includes an inner sleeve received within the outer sleeve and defining an inner conduit within the outer conduit to form a protective covering. The inner sleeve is split longitudinally. Portions of the inner sleeve on opposite sides of the split are coupled to one another so that a diameter of the inner conduit is adjustable in response to forces exerted thereon by one of BTD and tissues surrounding the outer sleeve.

Abstract: A method of fusing a sacroiliac joint including a sacrum, an ilium, and a sacroiliac joint space defined therebetween. The method may include: approaching a posterior aspect of the sacroiliac joint space with a joint implant including a body extending a length between a distal end and a proximal end; and delivering the joint implant into the sacroiliac joint space such that the joint implant passes through an access region defined between the posterior superior iliac spine and the posterior inferior iliac spine. The joint implant may be oriented in the sacroiliac joint space such that a portion of the body of the joint implant is positioned within a joint plane of the sacroiliac joint space, and such that the distal end of the joint implant is positioned posteriorly of an anterior boundary of the sacroiliac joint space.

Abstract: A bone fusion device includes a first anchor for insertion into a hole formed in a first phalange, and a second anchor for insertion into a hole formed in a second phalange. A rod includes a handle and a distal end, with the distal end being associated with each of the first anchor and the second anchor. The rod includes a breakaway portion between the handle and the distal end allowing the handle to be manually separated from the distal end.

Abstract: A method for locating a material having thermoplastic properties in pores of bone tissue includes providing a pin having the material having thermoplastic properties and a core, wherein the material having thermoplastic properties is arranged on the circumferential surface of the core constituting an outer region of the pin. An opening is provided in the bone tissue, and the pin is positioned at least partly in the opening. The outer region of the pin is then impinged with mechanical vibration energy for a time sufficient for liquefying at least part of the material having thermoplastic properties, and, in a liquefied state, pressing it into the pores of the bone tissue surrounding the opening. The vibration energy is stopped for a time sufficient for re-solidification of the liquefied material, and then the core is removed.

Abstract: Some embodiments of the invention provide an apparatus that (1) delivers a fusion member between two vertebral bodies after at least a portion of the fibrocartilaginous disc between the vertebral bodies has been removed, and (2) affixes the fusion member to the vertebral bodies. In some embodiments, the apparatus includes (1) a fusion member that is delivered and positioned between the vertebral bodies, (2) a delivery mechanism that delivers and positions the fusion member between the vertebral bodies, and (3) an anchoring member that affixes the fusion member to the vertebral bodies.

Abstract: A method for locating a material having thermoplastic properties in pores of bone tissue includes providing a pin having the material having thermoplastic properties and a core, wherein the material having thermoplastic properties is arranged on the circumferential surface of the core constituting an outer region of the pin. An opening is provided in the bone tissue, and the pin is positioned at least partly in the opening. The outer region of the pin is then impinged with mechanical vibration energy for a time sufficient for liquefying at least part of the material having thermoplastic properties, and, in a liquefied state, pressing it into the pores of the bone tissue surrounding the opening. The vibration energy is stopped for a time sufficient for re-solidification of the liquefied material, and then the core is removed.

Abstract: Spinal implants and methods for spinal stabilization and/or fusion are provided. Exemplary implants described herein can be configured for delivery to a facet joint to stabilize and/or fuse the facet joint, and can optionally be anchored within the pedicle for added fixation. The implant can optionally include a fusion-promoting bioactive material thereby providing a single device capable of spinal stabilization and/or fusion. Furthermore, a method of placing such an implant within a facet joint is provided.

Abstract: Anchoring devices, anchoring systems for intervertebral implants, intervertebral implants, and instruments and methods for implanting implants are disclosed. In preferred configurations, these various objects share the feature of comprising or cooperating with an anchoring device having a body comprising at least one curved plate elongated along a longitudinal axis, designed to be inserted through a passage crossing at least a part of implant, in order to penetrate into at least one vertebral endplate and attach implant onto this vertebral endplate by means of at least one stop retaining the implant, characterized in that the body comprises at least one longitudinal rib on at least a part of at least one of its faces, said rib being designed to cooperate with a groove made in passage of implant. In some preferred configurations, anchoring device comprises withdrawal stops or latches, and/or means for withdrawing the anchor from an inserted position.

Abstract: A posterior spinal fastener is disclosed for insertion into a vertebra of a mammalian body, the vertebra having posterior elements and a vertebral body. The fastener includes an elongate member adapted for insertion into the vertebra. The elongate body has an anterior portion and a posterior portion. The anterior portion is arcuate in shape for placement in the vertebral body. The posterior portion has a length so as to be accessible at the posterior elements of the vertebra when the anterior portion is disposed in the vertebral body. A method of use of the posterior spinal fastener is also disclosed, in which the posterior spinal fastener is introduced into the vertebra at the posterior elements and arcuately extended into the vertebral body.

Abstract: The present invention provides an orthopaedic implant including a base device having a device surface and a fixation material attached to at least one portion of the device surface. The fixation material is configured to provide a minimally sufficient adhesive force to resist natural pull out caused by forces acting on the base device after implantation and bone growth. Also provided is a method of manufacturing an orthopaedic implant. A base device with a device surface is provided and a minimally sufficient adhesive force, that can resist natural pull out caused by forces acting on the base device after implantation and bone growth, is determined. A proper amount of fixation material sufficient to provide an adhesive force equal to the minimally sufficient adhesive force is determined and fixation material is applied to the device. When the proper amount of fixation material is applied to the device surface, application is stopped.

Abstract: At least one bone fixation device comprising a stem having a maximum outer diameter is inserted into the sacroiliac joint through a minimally invasive incision path sized approximately at or about the maximum outer diameter of the stem in soft tissue, into the iliac bone, across the sacroiliac joint and into the sacrum. The stem is inserted through the incision path to a position within the sacroiliac joint between the iliac bone and the sacrum, to fuse the sacroiliac joint, without invasive joint preparation, removal of cartilage, or scraping at or near the sacroiliac joint. Desirably, at least a portion of the stem includes a surface permitting bony in-growth.

Abstract: An implantation device for fixating a bone has a main body. The main body has a peripheral region and comprises a polymeric material. The peripheral region comprises the polymeric material and a plasticizer. In particular, the peripheral region may be adapted to be fixed to a bone. A method for producing the implantation device includes the steps of forming an implantation device using polymer material, and dipping at least a portion of the implantation device into a plasticizer in such a way that a peripheral region of the implantation device is plasticized.

Abstract: Surgical fasteners, including tacks are disclosed for fastening a surgical mesh to underlying tissue during surgical procedures to repair body tissue, such as in hernia repair. Such tacks can include a head, a elongated body portion having a distal end and a proximal end, and an anchoring element on an outer surface of the body portion for inhibiting the removal of the tack from the mesh and body tissue.

Abstract: An implantation pin for implantation in a target structure has a pinhead and a shaft. The pinhead comprises a pinhead moulding portion comprising a moldable material which can be liquefied by application of mechanical energy such as ultrasonic vibration energy. A channel extends through the pinhead and the shaft, the channel connecting the pinhead molding portion to a discharge opening located at the shaft. The moldable material can be liquefied by applying mechanical energy in the form of ultrasonic vibrations via a fixation device including an ultrasonic sonotrode and a vibrating tip. The pressure applied by the vibrating tip can be transmitted via the border of the pinhead to the target structure while the liquefied mouldable material can be forced through the channel and the discharge opening into a gap between the implantation pin and a recess in a target structure thereby fixing the implantation pin in the target structure.

Abstract: A lockable pin plate assembly which has a pin plate adapted to be secured to stable bone and provided with pin holes for pins for pinning an unstable bone fragment. One or more pin holes are engageable by pins of an integral U-pin. The pins have stop surfaces thereon which are resiliently displaced when the pins are seated to automatically and self-lock the pin and the pin plate to oppose withdrawal and backing out of the pins from the pin plate. In a preferred embodiment, each pin of the U pin has a leading portion and a trailing portion, the leading portion being of smaller diameter to pass freely through an elliptical hole in the pin plate whereas the trailing portion is of larger size to become locked in the pin hole as it is advanced therein.

Abstract: A suture system has a suture with a first plurality of barbs located adjacent to a first end and a second plurality of barbs located adjacent to a second end, and a body located between the first plurality of barbs and the second plurality of barbs. The body provides an anchor that can hold tissue relative to the first end and the second end of the suture. The body can slide and be positioned on said suture.

Abstract: A surgical fastener system includes a plurality of fasteners having a throughbore with a non-circular cross section portion. The fasteners may engage with a splined mandrel that passes through the throughbore of the fasteners and rotates the fasteners relative to the mandrel to move at least one of the fasteners along the mandrel, e.g., along the mandrel's longitudinal axis. A distal end of the mandrel may be inserted into a material, such as a tissue, prosthetic or other, and a fastener may be deployed from the distal end of the mandrel while the distal end is positioned in the material.

Abstract: A suture system has a plurality of double ended barbed sutures each with a first plurality of barbs located adjacent to a first end and a second plurality of barbs located adjacent to a second end, and a body connector that connects said plurality of double ended barbed sutures. The body connector is located between the first plurality of barbs and the second plurality of barbs on each of the sutures. The sutures can move relative to the body connector. The body connector can retain tissue.

Abstract: A device for temporarily splinting toes, especially for the treatment of hammertoes and other defective positions of toes, consisting of a tube composed of a bio-absorbable material and a guide wire. The tube has an inner diameter of d, whereas the guide wire has an external diameter D, such that D<d. The device enables contact between the ball of the toe and the floor to be reestablished.

Abstract: Implant for stabilization of pelvic ring fractures, comprising a nail for intraosseous implantation, a fixing agent and at least one locking element for relative fixation of the pelvic bone to the nail.

Abstract: An orthopedic pin is used in a fixation device for treating fractures. The device has a body with holes to accept the pins. The pins have a layer of bioresorbable material thereon. Engagement between the pins and the body is initially through the bioresorbable material, which engagement rigidly fixes the relative angular orientation between the pins and the body when the device is applied to a bone. As the bioresorbable material is resorbed, the angular relation between the pins and the body is no longer rigidly fixed, thereby effecting a transformation from rigid osteosynthesis to flexible osteosynthesis to allow micromotion between the bone fragments which promotes healing.

Abstract: The present disclosure provides methods and devices that allow for rotational control, compression and fusion of the ankle as required for treatment while providing additional mobility in the movement of the foot. The devices of the present disclosure are configured to go through the talus and tibia for fusion of ankle joint while avoiding the calcaneus and subtalar joint. According to a first aspect, exemplary embodiments of the present disclosure are curved to provide sufficient area for rotational control and compression of the ankle bones. According to a second aspect, exemplary embodiments of the nails of the present disclosure are configured to be placed at an angle with respect to the intramedullary canal.

Abstract: A composite skull pin. The composite skull pin includes a core comprising a cone terminating in a distal point, the core being formed out of a substantially radiotranslucent material; and a jacket comprising a hollow cone terminating in a sharp distal point, the hollow cone of the jacket being sized and shaped so that it overlies, and closely conforms to, the exterior of the cone of the core. The jacket is formed out of a strong, hard material, and has a sufficiently small mass such that the composite skull pin has a low X-ray signature.

Abstract: A pin assembly for operation includes a hollow pin for operation having a plurality of side holes defined through an outer surface thereof and a head which is closed or open due to the presence of a through-hole; a hollow support having a pin fastening part formed therein in the shape of a groove to fasten one end of the pin for operation, and being open at both ends thereof, and a hollow injector for insertion into an insertion hole formed in the support, wherein the hollow pin for operation is fastened to the pin fastening part of the support, and by applying external force to one end of the support, the hollow pin for operation is inserted into a bone.

Abstract: A device and method for fixation of bone fractures has a bone screw comprising a shank with a threaded end portion, on the outer surface. The screw has a through bore with two bore portions differing in diameter. A step in the diameter is formed between these bore portions and is located within the end of the screw having the thread. This step in diameter can support a metal insert which in turn supports a polymer pin when the latter if pressurized with a sonotrode in the bone screw. Together with an applied ultrasonic vibration the pressure fluidizes the polymer pin and presses the material through holes configured in the wall of the bone screw and into surrounding bone.

Abstract: A substantially radiolucent cranial stabilization pin is adapted for use with a fixture for immobilizing a patient's head during a medical procedure. The pin includes a tip and a body, which are secured together to form the pin. The tip and body are constructed from non-ferrous, non-magnetic materials that are biocompatible. The tip and body are safe for use with, and compatible with, imaging techniques including MR imaging and CT imaging. In some examples the tip is a titanium insert and the body is molded within and around at least a portion of the tip. In some versions, the tip includes a hollow portion and one or more openings providing access to the hollow portion. The molded body flows into and around portions of the tip creating a secure pin suitable to withstand torque and axial forces observed in use.

Abstract: Suprapatellar systems, system components, and methods of operating on a tibial fracture of a patient are disclosed. A method can include making an incision proximal to a patella of a knee joint, forming an operation space, and inserting a portion of a retractor in the operation space to define an entry canal. The retractor can be inserted in a low profile configuration and, once positioned as desired by a surgeon, expanded to a high profile configuration. Expansion of the retractor can expand the operation space in at least one of an anterior-posterior direction or a medial-lateral direction and can increase a diameter of the entry canal. The method can further include inserting a trocar, having at least one guide hole, in the entry canal and guiding a guide pin through the at least one guide hole and into a tibia.

Abstract: An implantation pin for implantation in a target structure has a pinhead and a shaft. The pinhead comprises a pinhead molding portion comprising a moldable material which can be liquefied by application of mechanical energy such as ultrasonic vibration energy. A channel extends through the pinhead and the shaft, the channel connecting the pinhead molding portion to a discharge opening located at the shaft. The moldable material can be liquefied by applying mechanical energy e.g. in the form of ultrasonic vibrations via e.g. a fixation device including an ultrasonic sonotrode and a vibrating tip. The pressure applied by the vibrating tip can be transmitted via the border of the pinhead to the target structure while the liquefied moldable material can be forced through the channel and the discharge opening into a gap between the implantation pin and a recess in a target structure thereby fixing the implantation pin in the target structure.

Abstract: An implantation pin for implantation in a target structure has a pinhead and a shaft. The pinhead comprises a pinhead moulding portion comprising a moldable material which can be liquefied by application of mechanical energy such as ultrasonic vibration energy. A channel extends through the pinhead and the shaft, the channel connecting the pinhead molding portion to a discharge opening located at the shaft. The moldable material can be liquefied by applying mechanical energy in the form of ultrasonic vibrations via a fixation device including an ultrasonic sonotrode and a vibrating tip. The pressure applied by the vibrating tip can be transmitted via the border of the pinhead to the target structure while the liquefied mouldable material can be forced through the channel and the discharge opening into a gap between the implantation pin and a recess in a target structure thereby fixing the implantation pin in the target structure.

Abstract: A lockable pin plate assembly which has a pin plate adapted to be secured to stable bone and provided with pin holes for pins for pinning an unstable bone fragment. One or more pin holes are engageable by pins of an integral U-pin. The pins have stop surfaces thereon which are resiliently displaced when the pins are seated to automatically and self-lock the pin and the pin plate to oppose withdrawal and backing out of the pins from the pin plate. In a preferred embodiment, each pin of the U pin has a leading portion and a trailing portion, the leading portion being of smaller diameter to pass freely through an elliptical hole in the pin plate whereas the trailing portion is of larger size to become locked in the pin hole as it is advanced therein.

Abstract: A system for spinal surgery includes a prosthesis comprising a plurality of bone anchors which engage an intervertebral construct for fusion or motion preservation. The fusion construct comprises a spacer optionally encircled by a jacket. The motion preservation construct may comprise an articulating disc assembly or an elastomeric disc assembly. Any of the constructs may occupy the intervertebral disc space between adjacent vertebrae after removal of an intervertebral disc. The anchors slidingly engage the construct to securely fix the prosthesis to the vertebrae. The anchors and jacket of the fusion construct provide a continuous load path across opposite sides of the prosthesis so as to resist antagonistic motions of the spine.

Abstract: The present invention provides devices, systems and methods for anchoring medical devices to hard tissues, such as bones or bony structures, particularly vertebrae. By anchoring these medical devices directly to the surrounding hard tissue, the devices are anchored closer to the source of treatment. This provides additional stability and reduces migration of the device at the treatment site. Also, by attaching to hard tissue rather than soft tissue, a stronger attachment is often able to be made.

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.

Abstract: A bone fixation system and method are provided. The system includes a dual prong pin and a bone screw. The pin is especially configured and contoured to fixate fractures of the proximal phalanx, especially hyperextension fractures. Fracture of other long bones of the hand, foot or elsewhere may be managed with this bone fixation system.

Abstract: A device for reducing migration of a pin of an intramedullary fixation device, especially to reduce migration of a clavicle pin introduced in the medullary canal of the clavicle to fix a fractured clavicle bone. A clavicle nail with a curved tip is inserted within the medullary canal of the clavicle. The back end of the nail that extends out of the clavicle is provided with indentations or grooves. The back end of the nail is received in a hollow cavity of a cap, which locks onto the indentations or grooves of the nail. A screw is placed through an eyelet of the cap and turned into the clavicle to secure the cap to the clavicle. As a result, the nail is fixed within the medullary canal and undesirable migration of the pin within the medullary canal is reduced.

Abstract: An arthrodesis anchor as a monolithic piece has prongs supporting barbs extending radially therefrom. A neck between the ends may be angled to accommodate final alignment of resected surfaces of joints to be bonded. The neck may receive a tool for buttressing a first inserted end against further penetration into a joint while the second inserted end is inserted into the other adjacent joint. The proximal and intermediate phalangeal joints may be trimmed and pilot drilled, and may be broached with or without a k-wire guide. A first end may be inserted by a tool, typically into the proximal joint, but the order may be reversed. The second end may then be inserted into a pilot in the base of the intermediate joint.

Abstract: An implant includes a section made of polymer, wherein at least a portion of the section has a layer of a polymerizable and/or cross-linkable material. A method for fixation of a bone plate having several plate holes using the implant includes removing a cover sheet protecting the layer of polymerizable and/or cross-linkable material, activating the layer of polymerizable and/or cross-linkable material with electromagnetic energy or with moisture, introducing the implant into one of the plate holes of the bone plate when the bone plate is positioned on a bone, pressing on an end of the implant in order to contact the activated layer of polymerizable and/or cross-linkable material with the bone underneath the bone plate, and allowing the activated and pressurized layer of polymerizable and/or cross-linkable material to polymerize and/or cross-link and to adhere to the bone.

Abstract: A device and method for providing antimicrobial activity around a surgical implant. Antimicrobial activity is provided by the inclusion of a highly conductive material to a surgical implant and providing a low electrical charge to the implant. Electrical charge is provided by a static generator or battery attached to the implant or attached via electrical leads.

Abstract: A tracking device for an intramedullary pin whose spatial position is determined and/or tracked in image-guided surgery, including a reference device at a proximal end of the intramedullary pin and a medical navigation system which locates the reference device and determines the orientation of the intramedullary pin from the proximal end. A deformation detection device detects deformations of the intramedullary pin and communicates the deformations to the navigation system. Also provided is a tracking method for determining or tracking the spatial position of an intramedullary pin in image-guided surgery, and to an intramedullary pin that includes a deformation detection device.

Abstract: A surgical tool includes first and second K-wire components that are configured to pivot relative to each other and their relative position can be securely locked. The locking mechanism may be a sleeve, a retention ring or a collet.

Abstract: A surgical device (100) for guiding a key wire during a shoulder arthroplasty procedure, comprising a guide (105) for guiding a key wire (160) during the process of drilling into a scapula, and clamp means (101) configured to engage with the scapula neck such that a key wire located in the guide is located in a predetermined geometrical relationship with the scapula neck.

Abstract: A system for the percutaneous stabilization of adjacent vertebrae includes a plurality of elongated stabilization devices. Each stabilization device includes a radius of curvature. Each stabilization device further includes a leading end and a trailing end wherein the leading end is pointed for penetration through a vertebral body.

Abstract: A bone fixation system and method are provided. The system includes a dual prong pin and a bone screw. The pin is especially configured and contoured to fixate fractures of the proximal phalanx, especially hyperextension fractures. Fracture of other long bones of the hand, foot or elsewhere may be managed with this bone fixation system.