Abstract: Bone plates and methods of using the bone plates for adjoining bone fragments are disclosed herein. A device for adjoining at least two bone fragments includes a delivery catheter having an elongated shaft with a proximal end, a distal end, and a longitudinal axis therebetween, wherein the delivery catheter has an inner void for passage of at least one filling material and an inner lumen for passage of a light source; a conformable bone plate releasably engaging the distal end of the delivery catheter, wherein the conformable bone plate has a first surface, a second surface, a proximal end, and a distal end and at least one aperture extending from the first surface to the second surface for receiving a fastener; and an adapter releasably engaging the proximal end of the delivery catheter for receiving the light source and a delivery system housing the at least one filling material.

Abstract: The invention relates to an intramedullary linkage device for treatment of peri-prosthetic long bone fractures, system for long bone fracture treatment in the setting of pre-existing intramedullary implant using an intramedullary linkage device and intramedullary fracture fixation device, and methods of treating peri-prosthetic long bone fracture in the setting of pre-existing intramedullary implant using an intramedullary linkage device and intramedullary fracture fixation device.

Abstract: A surgical nail for treating a fractured bone includes a nail body extending along a longitudinal axis from a trailing end to a leading end and including a trailing end locking aperture extending transversely through a trailing end portion thereof and a leading end locking aperture extending transversely through a leading end portion thereof; a trailing end connecting element located at the trailing end of the nail body adapted and configured to be coupled to a trailing end aiming guide; and a leading end connecting element at the leading end of the nail body adapted and configured to be coupled to a leading end aiming guide.

Abstract: An intramedullary fixation system is configured to be fixed to first and second bone segments that are separated by a defect. The system includes an intramedullary fixation member that includes first and second wire segments that are twisted about each other so as to define a plurality of intersections. A distal one of the intersections is separable, such that rotation of the fixation device in a medullary canal causes bone material in the medullary canal to apply a counterforce to the wire segments that causes the distal intersection to separate, thereby driving respective distal ends of the wire segments into the bone segment, such that subsequent movement of the intramedullary fixation member a toward the first bone segment causes the second bone segment to move toward the first bone segment. The intramedullary fixation system can further include a fixation clip that anchors the intramedullary fixation member to the first bone segment.

Abstract: Apparatus and method for repairing a fractured bone. The apparatus and methods may involve an intramedullary rod. The rod may include a first elongated member and a second elongated member. Each of the first and second elongated members may be configured to bend in a first direction and to resist bending in a second direction. The first and second elongated members may be arranged such that: (1) the rod is bendable when the first direction of the first elongated member is aligned with the first direction of the second elongated member; and (2) the rod is rigid when the first direction of the first elongated member is aligned with the second direction of the second elongated member. Some embodiments may include rods that have sections that may be configured to be curved and rigid.

Abstract: An implant insertion device including a body having a first portion for coupling to a proximal end of an intramedullary rod and a second portion extending in a spaced position from the intramedullary rod in the vicinity of an aperture in a proximal end of the rod when the rod is coupled to the first portion. The second portion can include a targeting assembly having a passageway for receiving a guide sleeve and for pivoting the guide sleeve relative to the aperture through an angular range for inserting the fastener into the aperture of the rod. An implant insertion device for use with an implantable device is additionally provided.

Abstract: The present disclosure relates to systems and methods for installing shape memory polymers relative to orthopedic implants.

Abstract: A femur fixation device including an elongated nail configured for insertion into the medullary canal of the femur and a buttress element extending from the elongated nail. The buttress element is configured to reinforce the lesser trochanter region of the femur and assist in stabilizing the head portion of the femur.

Abstract: A soft tissue fixation system, most typically applicable to orthopedic joint repairs, such as anterior cruciate ligament (ACL) knee repair procedures, comprises an implant which is placeable in a tunnel disposed in a portion of bone, wherein the tunnel is defined by walls comprised of bone. A first member is deployable outwardly to engage the tunnel walls for anchoring the implant in place in the tunnel, and a second member is deployable outwardly to engage tissue material to be fixed within the tunnel. The second member also functions to move the tissue material outwardly into contact with the tunnel walls to promote tendon-bone fixation. Extra graft length is eliminated by compression of the tendon against the bone at the aperture of the femoral tunnel, which more closely replicates the native ACL and increases graft stiffness. The inventive device provides high fixation of tendon to bone and active tendon-bone compression.

Abstract: In one embodiment, the present invention includes an intramedullary osteosynthesis or arthrodesis implant including a central body, a first pair of legs extending from the central body to a pair of leg tips, and a second pair of legs extending from the central body, in a direction opposite the first pair of legs, to a pair of leg tips such that the central body, first pair of legs and second pair of legs are positioned alongside a longitudinal axis.

Abstract: This invention relates generally to devices, systems and methods for the internal fixation of bone fractures, and particularly, to intramedullary fracture fixation devices such as those used in, for example, the treatment of long bone fractures. An IM rod preferably is provided with multiple curved sections in different planes preferably designed to conform with the long bones of a patient, both during insertion and in the rod's final position in the long bone. In addition, the overlap of portions of the curved sections results in a co-planar curvature of portions of the IM rod which assist in the insertion process by guiding the proper rotation of the IM rod as it is inserted into the bone. Spiraling flutes extending down the distal portion of the rod also assist in properly guiding and orienting the rod about its longitudinal axis during insertion such that the appropriate segment of the curved rod conforms with the appropriate portion of the long bone at the appropriate place.

Abstract: A method and apparatus for reducing the incident of infection proximate to an exit site where a prosthesis fastener, e.g., a bone screw, percutaneously penetrates a patient's skin/soft tissue. Infection reduction is achieved in accordance with the invention by growing a tissue integrating seal around the fastener proximate to the exit site.

Abstract: A bone fixation device is provided with an elongate body having a longitudinal axis and having a first state in which at least a portion of the body is flexible and a second state in which the body is generally rigid, an actuateable gripper disposed at one or more locations on the elongated body, a hub located on a proximal end of the elongated body, and an actuator operably connected to the gripper(s) to deploy the gripper(s) from a retracted configuration to an expanded configuration. Methods of repairing a fracture of a bone are also disclosed. One such method comprises inserting a bone fixation device into an intramedullary space of the bone to place at least a portion of an elongate body of the fixation device in a flexible state on one side of the fracture and at least a portion of a hub on another side of the fracture, and operating an actuator to deploy at least one gripper of the fixation device to engage an inner surface of the intramedullary space to anchor the fixation device to the bone.

Abstract: A femoral instrument for use in the intramedullary canal is described and includes an intramedullary rod having a tip at a free end. A body is attached to the intramedullary rod and has a face with a bone abutting portion. A centraliser mechanism is located within the rod and is operable to deploy and retract a plurality of members to engage and disengage an inner surface of the intramedullary canal.

Abstract: An intramedullary nail for use in a medullary canal of an epiphysis and a diaphysis of a long bone is provided. The nail includes a body having a length in a longitudinal direction and a width in the transverse direction normal to the longitudinal direction. The body has a diaphyseal portion and a first epiphyseal portion. The diaphyseal portion has an external periphery configured for placement in the medullary canal of the diaphysis of the long bone. The diaphyseal portion defines a longitudinally extending first surface of the diaphyseal portion. The first surface defines a longitudinally extending first void. The first epiphyseal portion extends from the diaphyseal portion. The first epiphyseal portion is configured for placement in the medullary canal of the first epiphysis of the long bone. The nail also includes a first insert positioned in the longitudinally extending first void of the diaphyseal portion. The first insert and the diaphyseal portion of the body are made from different materials.

Abstract: Among other things, there are disclosed embodiments of an intramedullary nail system for use in pediatric cases, including an intramedullary nail and a targeting assembly. Embodiments of the nail may be one-piece and include a proximal portion, a medial portion and a distal portion. The junction of the medial portion and distal portion is a bend that provides a small angle between the medial portion and the distal portion as viewed when the nail is substantially in a medial-lateral plane. The targeting assembly attaches to the proximal portion of the nail securely and enables easy insertion of fixing screws.

Abstract: Systems and methods for separating an internal bone fixation device from an introducer are disclosed. In some embodiments, a separation system includes a stabilizer configured to slide over an introducer for delivery of a bone fixation device to a bone cavity, the stabilizer being further configured to score a proximal end of the bone fixation device; and a separator configured to engage the introducer and to provide an impact to the introducer to separate the introducer from the bone fixation device.

Abstract: A controlled removable fracture-reducing assembly (10) for reducing a bone fracture. According to one embodiment of the present invention, a controlled removable fracture reducing assembly (10) includes an implant (12), a reducer (14), a buttress (16), and a locking device (18) that engage a proximal bone fragment (2) and a distal bone fragment (4). The implant (12) is secured to the distal bone fragment (4) by the locking device (18). The buttress (16) engages the implant (12) through an opening (30). The reducer (14) contains a compressing screw (24) that applies a force (60) on the buttress (16), reducing the fracture. According to another embodiment of the invention, the reducer (114) contains a cam mechanism (124) which applies a force (186) on the buttress (116), which does not engage the implant (112), that pushes the proximal bone fragment (102) to reduce the fracture.

Abstract: A controlled removable fracture-reducing assembly for reducing a bone fracture. According to one embodiment, a controlled removable fracture reducing assembly includes an implant, a reducer, a buttress, and a locking device that engage a proximal bone fragment and a distal bone fragment. The implant is secured to the distal bone fragment by the locking device. The buttress engages the implant through an opening. The reducer contains a compressing screw that applies a force on the buttress, reducing the fracture. According to another embodiment, the reducer contains a cam mechanism which applies a force on the buttress, which does not engage the implant, that pushes the proximal bone fragment to reduce the fracture. According to another embodiment, the reducer is a jacking mechanism that pushes the proximal bone fragment while pulling the implant and distal fragment to reduce the fracture.

Abstract: An intramedullary rod for use in a mammalian body comprising an elongate nail having a stem and a head and a threaded element carried by the head and accessible at the proximal end for rotation relative to the head. A locking mechanism coupled to the threaded element and configured to preclude rotation of the threaded element relative to the head when the locking mechanism is in a first position and permit rotation of the threaded element relative to the head when the locking mechanism is in a second position.

Abstract: A bone fixation device comprises an elongated body. The elongated body includes a first end portion with a coil and an opposite second end portion with an elongated tail. The second end portion also includes an attachment portion configured for engagement with a fastener.

Abstract: Systems, devices and methods are disclosed for treating fractures. The systems, devices and methods may include one or both of an implant, such as an intramedullary nail, and a fastening assembly, such as a lag screw and compression screw assembly. The implant in some embodiments has a proximal section with a transverse aperture and a cross-section that may be shaped to more accurately conform to the anatomical shape of cortical bone and to provide additional strength and robustness in its lateral portions, preferably without requiring significant additional material. The fastening assembly may be received to slide, in a controlled way, in the transverse aperture of the implant. In some embodiments, the engaging member and the compression device are configured so that the compression device interacts with a portion of the implant and a portion of the engaging member to enable controlled movement between the first and second bone fragments.

Abstract: An intramedullary drug delivery device is disclosed and can be inserted within a bone canal of a bone. The intramedullary drug delivery device can include a housing. A drug delivery region can be established along the housing. Also, the drug delivery region can be configured to substantially span a fracture within the bone.

Abstract: An intramedullary nail comprising an outer tubular sheath, a flexible rod and a driver element mobile within the sheath longitudinally with an engagement element formed out of the wall of the tubular sheath. After the nail has been inserted, distal end first, into the intramedullary cavity, the flexible rod is pulled, thereby engendering the driver element to advance the engagement element into the cortical bone, thus keeping the intramedullary nail in position within the intramedullary cavity.

Abstract: Devices and associated methods are disclosed for treating bone, and particularly bone tissue at the joints. Disclosed are implantable devices that can be used either alone or in combination with this augmentation or hardening material for the repair of bone defects and which are particularly suited for use at the joints, and even more particularly, suited for use at the subchondral bone level.

Abstract: A method and apparatus for forming any size antibiotic impregnated bone cement (AIBC) intramedullary (IM) nail. The cement nail is formed around a base support or base IM nail. The apparatus includes a molded plastic tube device to form the shape of the cement IM nail and plastic spacers which position the molded plastic tube around the base support or base IM nail for formation of the cement nail. The AIBC material may be any of the known antibiotic loaded/impregnated bone cements that are commercially available.

Abstract: A segmented intramedullary nail having an implantation state in which the segments are relatively moveable to permit conformation to the curvature of a bone during implantation, and a post-implantation state in which the segments are not relatively moveable, and in which the segments retain the configuration of the curvature of the bone. The nail may be radiolucent and/or contain radiopaque markings. It may be provided independently or as part of a kit with an implantation and a tightening tool. A cap and/or one or more sleeves may be provided to prevent bone in-growth at a point of coupling to an insertion tool and/or at the interface between segments.

Abstract: System, including methods, apparatus, and kits, for bone fixation with an articulated nail. The nail may have a first segment and a second segment that extend from respective opposite ends of the nail to a joint region that connects the segments. Each segment may define one or more transverse apertures configured to receive a fastener that attaches the segment to bone. The joint region may have a movable configuration that permits pivotal rearrangement of the segments relative to each other and a locked configuration that fixes the segments relative to each other.

Abstract: A surgical instrument system is described which comprises an alignment guide (6,100) comprising a body section having a through bore (50) defining a longitudinal axis (122); and a rod (40) comprising a cylindrical member (2) for insertion into the through bore; and a restraining system (46, 52, 48, 94) for preventing relative movement of the alignment guide and rod along the longitudinal axis, when the cylindrical member is inserted into the through bore, and the alignment guide is located towards the proximal end of the rod. The restraining system may comprise a resilient element (46) and a recess (52) configured to engage the resilient element. In a preferred embodiment, a resilient member is disposed on the surface of the rod. Such a system allows the alignment guide to be restrained towards the proximal end of the rod so that the rod can be inserted to a patient using one hand, rather than requiring two hands (one to secure the alignment guide relative to the rod and one to insert the rod).

Abstract: A universal targeting apparatus includes a generally U-shaped body having one end configured to be coupled to the proximal end of the intramedullary implant and a mounting portion at an opposite end of said body. An arm is rotatably mounted to the mounting portion of the U-shaped body and includes bores defined at its opposite ends. Each bore is arranged at a different angle to correspond to the angle of a transverse aperture in the intramedullary implant. The arm can be rotated so an appropriate one of the angled bores is aligned with the transverse aperture to serve as a guide for creating targeting holes in the bone.

Abstract: Intramedullary medical devices (e.g., intramedullary nails) and methods for their use and manufacture are described herein. The intramedullary medical devices described herein may provide sustained compressive forces across a bone fusion site despite bone resorption processes. Through various embodiments, the intramedullary medical devices described herein may provide non-linear force curves relative to displacement. Intramedullary medical devices are described with multiple elements made of different materials. Examples of intramedullary medical devices are described with shape memory alloys.

Abstract: Methods, systems and devices are provided for facilitating a surgical procedure on a knee, particularly, a revision total knee replacement procedure. Prior femoral and tibial prostheses are removed. A cut end of a distal femur is engaged with a femoral adjustment member, which will, typically center itself about an intermedullary rod placed into the femur. The lateral and medial, forces exerted by lateral and medial sides of the femoral adjustment member and the cut tibial plateau against each other are measured. The femoral adjustment member is adjusted to apply and/or adjust tension to the lateral collateral ligament and/or the medial, collateral ligament based on the measured forces, for example, such that the measured lateral force and the measured medial force are matched. Based on the position of the adjusted femoral member, guided clean-up cuts for placement of a new femoral prostheses are made on the cut end of the distal femur.

Abstract: A method for repairing a fractured bone includes providing a bone fracture fixation assembly including a plate, an elongated shaft, and a rod. At least a portion of the shaft is threaded, and the shaft has a hole extending therethrough. The hole has an axis transverse to a longitudinal axis of the shaft. The method further includes positioning the plate adjacent the surface of the fractured bone, extending the shaft into the bone, cooperatively engaging the threaded portion of the shaft with a screw receiving aperture of the plate, extending the rod into the bone, and inserting the rod into the hole of the shaft.

Abstract: Photodynamic bone stabilization systems are disclosed herein. In an embodiment, a photodynamic bone stabilization system includes a catheter having an elongated shaft with a proximal end adapter, a distal end releasably engaging an expandable portion, and a longitudinal axis therebetween; a light-conducting fiber configured to transmit light energy to the expandable portion; a light-sensitive liquid monomer comprising an initiator, wherein the initiator is activated when the light-conducting fiber transmits the light energy to initiate polymerization of the light-sensitive liquid monomer; and a cooling medium configured to control polymerization temperature, wherein the catheter comprises an inner void sufficiently designed to pass the light-sensitive liquid monomer into the expandable portion, and wherein the catheter comprises an inner lumen sufficiently designed to pass the light-conducting fiber into the expandable portion and configured to circulate the cooling medium.

Abstract: A drug-impregnated sleeve for encasing a medical implant is provided. In one embodiment, the sleeve may include a body made of a biologically-compatible material that defines an internal cavity configured to receive the medical implant. In one embodiment, the biologically-compatible material is bioresorbable. The body may include a plurality of apertures, such as perforations or holes, extending from the cavity through the body. The sleeve may further include a first end, a second end, and a drug impregnated into the resorbable sheet. In one possible embodiment, the first end of the sleeve may be open for receiving the medical implant therethrough and the second end may be closed. The implant may be encased in the sleeve and implanted into a patient from which the drug is dispensed in vivo over time to tissue surrounding the implantation site.

Abstract: An intramedullary device includes an intramedullary nail extending along a longitudinal axis from a proximal end to a distal end, a proximal portion of the intramedullary nail including a cavity extending from an opening at the proximal end along the longitudinal axis and a locking hole extending transversely therethrough along with a first insert sized and shaped for insertion into the cavity along the longitudinal axis thereof and including a transverse bore aligning with the locking hole.

Abstract: A bone fixation device is provided with an elongate body having a longitudinal axis and having a first state in which at least a portion of the body is flexible and a second state in which the body is generally rigid, an actuateable gripper disposed at one or more locations on the elongated body, a hub located on a proximal end of the elongated body, and an actuator operably connected to the gripper(s) to deploy the gripper(s) from a retracted configuration to an expanded configuration. Methods of repairing a fracture of a bone are also disclosed. One such method comprises inserting a bone fixation device into an intramedullary space of the bone to place at least a portion of an elongate body of the fixation device in a flexible state on one side of the fracture and at least a portion of a hub on another side of the fracture, and operating an actuator to deploy at least one gripper of the fixation device to engage an inner surface of the intramedullary space to anchor the fixation device to the bone.

Abstract: An ankle fusion device has a proximal portion generally aligned with a first longitudinal axis. The proximal portion includes a proximal end and a first fastener hole. The proximal portion has an arcuate curve such that the proximal end is spaced a distance from the first longitudinal axis in a first direction. The first fastener hole is configured to receive a first fastener along a first fastener axis. A distal portion of the ankle fusion device extends to a distal end from the proximal portion along a second longitudinal axis. The second longitudinal axis is angled in second and third directions relative to the first longitudinal axis. The second direction is perpendicular to the first direction and the third direction being opposite the first direction. The distal portion includes a second fastener hole configured to receive a second fastener along a second fastener axis.

Abstract: A bone fixation device includes an elongated body (a) having a first channel extending therethrough and configured for insertion into a bone, a first opening (b) formed on a first side wall of the body, the first side wall facing a lateral direction when implanted in a target orientation within the bone and a second opening (c) formed on a second side wall of the body opposite the first opening. A second channel (d) extends through the body from the first opening to the second opening and is dimensioned to permit insertion of an implant therethrough. A first bump (e) is positioned about a periphery of the first opening at a location at which a stress concentration would be a maximum if no such first bump were formed. The first bump is dimensioned to diffuse a concentration of stress about the periphery due to forces applied thereto by an implant extending through the second channel.

Abstract: Apparatus and methods for bone fracture repair. The apparatus may include a structural support for positioning a first bone segment relative to a second bone segment. The apparatus may include an anchoring substrate. The anchoring substrate may be configured to compress the first bone segment to the second bone segment. The anchoring substrate may transmit tension from a distal bone segment anchor in the first bone segment to a proximal bone segment anchor in the second bone segment. The apparatus may be configured to be deployed percutaneously in an inner cavity of a bone. The apparatus may be installed in an open fracture. The apparatus may be expanded, self-expanding or configured for mechanically actuation. Some embodiments of the apparatus may include a central axis member that may be used in conjunction with expansion of one or both of the structural support and the anchoring substrate to configure the apparatus.

Abstract: Methods and apparatus for installing intramedullary medical devices (e.g., intramedullary nails) are described herein. Intramedullary medical devices in accordance with this disclosure provide sustained compressive forces across a bone fusion site despite bone resorption processes. Intramedullary medical devices in accordance with this disclosure include pseudo-elastic shape memory alloys containing nickel and titanium. Portions of intramedullary medical devices, including shape memory alloy elements in the intramedullary medical devices, may have strains imparted upon them through the methods and apparatus described herein. Further aspects of surgery techniques are also performed and controlled through the methods and apparatus described herein.

Abstract: An expandable rod is provided that is sized for insertion into a patient's bone. A method for using the expandable rod to prepare the patient's bone to receive an orthopedic implant is also provided. The expandable rod is adjustable between a first, contracted state and a second, expanded state, the expansion member expanding radially outwardly from the contracted state to the expanded state.

Abstract: In one embodiment the present invention is an implant suitable for implantation in bone, comprising a median zone extending along a longitudinal axis between a first end and a second end, the first end having a face extending generally perpendicular to the axis to form an abutment having a width; and a first fixation zone extending from the first end and the abutment, the first fixation zone including a pair of tabs formed of shape-memory material extending from a base portion of the tabs adjacent the abutment such that the abutment extends further from the axis in a radial direction than the base portion of the tabs, wherein the pair of tabs are separable from one another by shape-memory action at body temperature.

Abstract: Among other things, there are disclosed embodiments of an intramedullary nail system for use in pediatric cases, including an intramedullary nail and a targeting assembly. Embodiments of the nail may be one-piece and include a proximal portion, a medial portion and a distal portion. The junction of the medial portion and distal portion is a bend that provides a small angle between the medial portion and the distal portion as viewed when the nail is substantially in a medial-lateral plane. The targeting assembly attaches to the proximal portion of the nail securely and enables easy insertion of fixing screws.

Abstract: A locking rod fusion device and method uses internal locking rods and screws that will lock together. In particular, the device allows the insertion of multiple locking rods in combination with a plate, which requires less dissection and disruption of soft tissues and vasculature. The device also provides a more stable internal construct for fusions that prevent non-unions, hardware failure and reoccurrence of deformities, such as Charcot foot. The device combines the strength of locking technology and the utility and ease of an internal rod system to provide a single stable construct in multiple planes as apposed to using multiple plates or screws separately.

Abstract: The present bone implant is a cannulated screw/nail or combination having end, middle and head threads as well as unthreaded portions along the length of the shaft. The pitch of the head threads is always less than the middle threads. Variations include a two-part construction with a narrow protrusion having narrow-protrusion threads of opposite hand, or the inclusion of at least first middle threads and second middle threads of different pitch. The implant provides bone compression engineering heretofore unavailable with prior known compression screws.

Abstract: A supporting instrument with a modular intramedullary nail includes a plurality of intramedullary nails and a coupling module. Each intramedullary nail is in a form of a long rod and has a coupling portion arranged between two ends of the intramedullary nail and an abutting surface along a longitudinal face of the intramedullary nail. The coupling module is mounted to the coupling portions of the plurality of intramedullary nails for the abutting surfaces of the plurality of intramedullary nails to abut against each other and for assembling the plurality of intramedullary nails.

Abstract: The present invention discloses a system for securing at least one fastener to an implant. At least one adhesive capsule is inserted in a recess preferably located along a longitudinal axis of the implant. The at least one adhesive capsule may be inserted in the recess and held in place therein by a holder. A plurality of adhesive capsules and holders may be inserted in one or more recesses located substantially along the longitudinal axis of the implant. The at least one adhesive capsule preferably has a casing housing an adhesive material configured to be pierced by the at least one fastener to secure the at least one fastener to an aperture of the implant. The casing of the adhesive capsule may form an annular passageway to receive a guide wire for aiding the insertion of the capsule in an implant having a longitudinal bore along at least a portion thereof.

Abstract: A supporting instrument with a modular intramedullary nail includes a plurality of intramedullary nails and a coupling module. Each intramedullary nail is in a form of a long rod and has a coupling portion arranged between two ends of the intramedullary nail and an abutting surface along a longitudinal face of the intramedullary nail. The coupling module is mounted to the coupling portions of the plurality of intramedullary nails for the abutting surfaces of the plurality of intramedullary nails to abut against each other and for assembling the plurality of intramedullary nails.

Abstract: The present invention relates to a nail and fastener assembly for use in providing a stable construct for optimal fixation of the hindfoot and to methods for implanting the nail and fastener assembly. One embodiment of the nail and fastener assembly provides additional fixation, for example, in the form of one or more threaded bores, to hold the fasteners in a fixed position. Another embodiment provides angled bores to allow multi-planar and multi-axial implantation of the fasteners. In some instances, the fasteners may cross one or more articulating surfaces of the foot. For example, the fastener may traverse one or more of the calcaneo-cuboid and the talo-calcaneal articulating surfaces to aid in more secure stabilization of the hindfoot.