Abstract: A bone plate includes first and second ends opposed along a longitudinal axis oriented along a longitudinal direction, first and second sides opposed along a lateral direction, and a bone-facing surface and an outer surface opposed along a transverse direction. The plate defines a first hole and a second hole arrangement extending from the outer to the bone-facing surface. The second hole arrangement is distal of the first hole, which is configured to receive a first fixation member, and the second hole arrangement is configured to receive at least one second fixation member for affixing with underlying bone. The plate is pivotable along an angulation range about the first hole. The second hole arrangement laterally crosses the longitudinal axis, defines the angulation range, and allows the at least one second fixation member to substantially secure the plate to the underlying bone at any angulation within the angulation range.

Abstract: A bone plate for treating periprosthetic fractures includes a head portion sized and shaped so that, in an operative position, a proximal end thereof aligns with a vastus ridge of a greater trochanter of a femur. The plate also includes a shaft portion extending distally from the head portion. The shaft portion includes offset holes to receive bone fixation elements therethrough. Each of the offset holes includes a first hole positioned on a first side of a longitudinal axis of the plate and a second hole positioned on a second side of the longitudinal axis opposite the first side so that bone fixation elements inserted therethrough extend anterior and posterior of a prosthetic received within the femur. The first and second holes are staggered relative to one another along a length of the shaft portion and extending beyond longitudinal edges of the shaft portion.

Abstract: A bone plate for treating periprosthetic fractures includes a head portion to be positioned along a greater trochanter of a bone. The head portion includes pairs of bone fixation element receiving openings extending therethrough from a first surface of the plate which, when the plate is in an operative position, faces away from the bone, and a second surface which, when the plate is in the operative position, faces toward the bone. A pair of cable holes extend through the head portion from a first longitudinal side connecting the first and second surfaces to a second longitudinal side connecting the first and second surfaces. The head portion includes a pair of hooks for engaging a superior ridge of the greater trochanter. The plate also includes a shaft portion extending distally from the head portion to extend along a portion of the bone distal of the greater trochanter.

Abstract: A bone plate for treating periprosthetic fractures includes a head portion to be positioned along a greater trochanter of a bone. The head portion includes pairs of bone fixation element receiving openings extending therethrough from a first surface of the plate which, when the plate is in an operative position, faces away from the bone, and a second surface which, when the plate is in the operative position, faces toward the bone. A pair of cable holes extend through the head portion from a first longitudinal side connecting the first and second surfaces to a second longitudinal side connecting the first and second surfaces. The head portion includes a pair of hooks for engaging a superior ridge of the greater trochanter. The plate also includes a shaft portion extending distally from the head portion to extend along a portion of the bone distal of the greater trochanter.

Abstract: A plate for treating a bone includes a plate body extending along a longitudinal axis from a first end to a second end and being sized, shaped and contoured to be positioned along a desired surface of a bone. The plate also includes a slotted opening extending through the plate body and defined by a first portion sized and shaped to permit a head portion of a bone fixation element fixed to the bone to be passed therethrough and a second elongated portion extending along the longitudinal axis from the first portion in communication with the first portion, the second portion sized to prevent the head portion of the bone fixation element from being passed therethrough so that, when the head portion of the bone fixation element is received through the first portion, the plate is slidable relative thereto such that the second portion engages the head portion of the bone fixation element.

Abstract: A bone plate for treating periprosthetic fractures includes a head portion sized and shaped so that, in an operative position, a proximal end thereof aligns with a vastus ridge of a greater trochanter of a femur. The plate also includes a shaft portion extending distally from the head portion. The shaft portion includes offset holes to receive bone fixation elements therethrough. Each of the offset holes includes a first hole positioned on a first side of a longitudinal axis of the plate and a second hole positioned on a second side of the longitudinal axis opposite the first side so that bone fixation elements inserted therethrough extend anterior and posterior of a prosthetic received within the femur. The first and second holes are staggered relative to one another along a length of the shaft portion and extending beyond longitudinal edges of the shaft portion.

Abstract: A bone plate for treating periprosthetic fractures includes a head portion to be positioned along a greater trochanter of a bone. The head portion includes pairs of bone fixation element receiving openings extending therethrough from a first surface of the plate which, when the plate is in an operative position, faces away from the bone, and a second surface which, when the plate is in the operative position, faces toward the bone. A pair of cable holes extend through the head portion from a first longitudinal side connecting the first and second surfaces to a second longitudinal side connecting the first and second surfaces. The head portion includes a pair of hooks for engaging a superior ridge of the greater trochanter. The plate also includes a shaft portion extending distally from the head portion to extend along a portion of the bone distal of the greater trochanter.

Abstract: A plate for treating a bone includes a plate body extending along a longitudinal axis from a first end to a second end and being sized, shaped and contoured to be positioned along a desired surface of a bone. The plate also includes a slotted opening extending through the plate body and defined by a first portion sized and shaped to permit a head portion of a bone fixation element fixed to the bone to be passed therethrough and a second elongated portion extending along the longitudinal axis from the first portion in communication with the first portion, the second portion sized to prevent the head portion of the bone fixation element from being passed therethrough so that, when the head portion of the bone fixation element is received through the first portion, the plate is slidable relative thereto such that the second portion engages the head portion of the bone fixation element.

Abstract: Systems and methods for measuring an intramedullary length for an orthopedic implant are described herein. A reamer system comprises a reamer shaft and a first reamer head. The reamer shaft comprises a proximal end having a drive coupler, a distal end having a reamer coupler, and markers located along the reamer shaft proximate the proximal end. The first reamer head comprises a head coupler configured to connect with the reamer coupler, and one or more cutting flutes located distal to the head coupler. The markers provide an indication of lengths of the system from a distal tip of the cutting flutes to each of the markers. The markers can be radiopaque. A method of employing the reamer system to measure the intramedullary length is described herein.

Abstract: A sterile wound treatment kit includes a plastic container pouch with a sealed outer periphery. A drug absorbing medium is located within the pouch interior. A syringe accepting fitting is located on the pouch for discharging a treatment drug from a syringe into the pouch interior shortly before treating a patient. The drug absorbing medium then contacts and absorbs the treatment drug. The pouch can be opened at the time of use to allow access to the drug absorbing medium so that the medium can be applied to a wound site. The pouch can also be equipped with a dispensing nozzle for dispensing the treatment medium.

Abstract: A sterile wound treatment kit includes a plastic container pouch with a sealed outer periphery which forms a sterile interior region which isolates the pouch interior from a surrounding environment. A drug absorbing medium is located within the pouch interior and initially isolated from the surrounding environment by the sealed periphery. A syringe accepting fitting is located on the pouch for discharging a treatment drug from a syringe into the pouch interior. The pouch interior is large enough to allow the drug absorbing medium to be shaken within the pouch interior once a drug is injected into the sterile interior region, whereby the drug absorbing medium will contact and evenly absorb the drug treatment. The pouch can be opened at the time of use to allow access to the drug absorbing medium so that the medium can be applied to a wound site.

Abstract: A sterile wound treatment kit includes a plastic container pouch with a sealed outer periphery which forms a sterile interior region which isolates the pouch interior from a surrounding environment. A drug absorbing medium is located within the pouch interior and initially isolated from the surrounding environment by the sealed periphery. A syringe accepting fitting is located on the pouch for discharging a treatment drug from a syringe into the pouch interior. The pouch interior is large enough to allow the drug absorbing medium to be shaken within the pouch interior once a drug is injected into the sterile interior region, whereby the drug absorbing medium will contact and evenly absorb the drug treatment. The pouch can be opened at the time of use to allow access to the drug absorbing medium so that the medium can be applied to a wound site.