Abstract: A substrate for use in an aqueous slurry has a polymeric coating to provide a compliant and sticky surface. The polymer coating has a chemical to render the surface hydrophobic so as to attract hydrophobic or hydrophobized mineral particles in the slurry. The substrate can take the form of a conveyor belt, a bead, a mesh, an impeller, a filter or a flat surface. The substrate can also be an open-cell foam. The polymeric coating can be modified with tackifiers; plasticizers; crosslinking agents; chain transfer agents; chain extenders; adhesion promoters; aryl or alky copolymers; fluorinated copolymers and/or additives; hydrophobizing agents such as hexamethyldisilazane; inorganic particles such as silica, hydrophobic silica, and/or fumed hydrophobic silica; MQ resin; and/or other additives to control and modify the properties of the polymer.

Abstract: A process of coating an open-cell foam substrate includes the steps of arranging two rollers separated by a gap; positioning the substrate above the gap; providing a coating material onto the substrate, feeding the substrate through the gap so as to achieve a layer of the coating material on the substrate, wherein the coating material is selected from the group consisting of a polysiloxane derivative, acrylic polymer, butyl rubber, natural rubber, nitriles, styrene block copolymers with ethylene, styrene block copolymers with propylene, styrene block copolymers with isoprene and polyvinyl ether and modifying the coating with tackifiers; plasticizers; crosslinking agents; chain transfer agents; chain extenders; adhesion promoters; aryl or alky copolymers; fluorinated copolymers; hexamethyldisilazane; and silica.

Abstract: A method of implanting a prosthetic component using bone density information comprises positioning a bone density reference proximate a patient, obtaining two-dimensional x-ray images of a bone of the patient including the bone density reference, determining a density of the bone from the bone density reference in the two-dimensional x-ray images, superimposing the density of the bone into a three-dimensional mean bone model to generate a patient-specific mean bone model, determining an interface between the bone and the prosthetic component based on bone density information of the patient-specific mean bone model, and implanting the prosthetic component in the bone at the interface. Determining the interface comprises evaluating bone density at the interface to place the prosthetic component, determining bone load threshold at the interface to avoid damaging the bone, and determining hardness for the prosthetic implant at the interface to avoid damaging the bone.

Abstract: The augments, systems and methods for supporting acetabular implants described herein can include an augment (100) for supporting an acetabular shell (90) having a first portion (136) of a locking mechanism. The system can also include a shell having a second portion of a locking mechanism (96). The first portion of the locking mechanism and the second portion of the locking mechanism can be adapted to move relative to one another from an unlocked state to a locked state to fixedly couple the augment to the shell. In some examples, the augment can be contourable to match the shape of a bone.

Abstract: A method of implanting a prosthetic component using bone density information comprises positioning a bone density reference proximate a patient, obtaining two-dimensional x-ray images of a bone of the patient including the bone density reference, determining a density of the bone from the bone density reference in the two-dimensional x-ray images, superimposing the density of the bone into a three-dimensional mean bone model to generate a patient-specific mean bone model, determining an interface between the bone and the prosthetic component based on bone density information of the patient-specific mean bone model, and implanting the prosthetic component in the bone at the interface. Determining the interface comprises evaluating bone density at the interface to place the prosthetic component, determining bone load threshold at the interface to avoid damaging the bone, and determining hardness for the prosthetic implant at the interface to avoid damaging the bone.

Abstract: An alignment plate can comprise a body having an exterior-facing surface and an implant-facing surface, at least one adjustable finger extending in a direction transverse to a plane defined by the body, and at least one patient-engaging surface positioned on the at least one adjustable finger. The adjustable finger can be adjustable to vary the distance between the patient-engaging surface and the implant-facing surface. The patient-engaging surface can be configured to engage a portion of a patient to align the alignment plate relative to the patient in a selected orientation. Additional apparatus, methods, and systems are disclosed.

Abstract: A method of preparing a surgical plan comprises video capturing a range of motion of an anatomic joint of a patient to obtain a range of motion video, registering the range of motion video to two-dimensional images of a skeleton of the patient, identifying potential impingement and stability issues in the anatomic joint based on the range of motion video, templating a prosthetic implant on two-dimensional images of the anatomic joint using the identified potential impingement and stability issues of the anatomic joint to obtain position and orientation data, and electronically saving the position and orientation data of the prosthetic implant for use with a surgical navigation system. A system for planning and performing a surgical procedure comprises a motion capture system, an x-ray system, an electronic modeling system, and a surgical navigation system.

Abstract: An alignment plate can be designed and formed based upon a known geometry of a subject, such as a human patient. The alignment plate can include various members, such as a plurality of fingers or legs, to contact the selected points of the anatomy. Based upon contact of the fingers at the selected points of the anatomy, the alignment plate can be aligned at a preselected or predetermined alignment with a portion of the anatomy, such as an acetabulum.

Abstract: An acetabular prosthesis is described that includes a shell having an outer surface and an inner surface, the outer surface defining an external shape. There is at least one through bore extending from the outer surface of the shell to the inner surface of the shell. At least one augment is configured to be positioned at least partially within the at least one through bore of the shell such that, in an assembled state, the shell and the at least one augment define a modified external shape.

Abstract: The augments, systems and methods for supporting acetabular implants described herein can include an augment (100) for supporting an acetabular shell (90) having a first portion (136) of a locking mechanism. The system can also include a shell having a second portion of a locking mechanism (96). The first portion of the locking mechanism and the second portion of the locking mechanism can be adapted to move relative to one another from an unlocked state to a locked state to fixedly couple the augment to the shell. In some examples, the augment can be contourable to match the shape of a bone.

Abstract: A guide for an implant site in bone. The guide includes a bone mating surface configured to engage a prepared bone surface at the implant site to position the guide at a predetermined orientation, and a patient-specific surface configured to engage a predetermined portion of a specific patient's natural anatomy to position the guide at the predetermined orientation.

Abstract: According to various embodiments, a trial system (100) and instruments can be used to assist in confirming that a planned procedure is achieved. In various embodiments, the trial or provisional portions can include markings (110) on a trial or provisional portion to compare to one or more implanted members to ensure an planned position is achieved.

Abstract: An acetabular prosthesis is described that includes a shell having an outer surface and an inner surface, the outer surface defining an external shape. There is at least one through bore extending from the outer surface of the shell to the inner surface of the shell. At least one augment is configured to be positioned at least partially within the at least one through bore of the shell such that, in an assembled state, the shell and the at least one augment define a modified external shape.

Abstract: An acetabular prosthesis is described that includes a shell having an outer surface and an inner surface, the outer surface defining an external shape. There is at least one through bore extending from the outer surface of the shell to the inner surface of the shell. At least one augment is configured to be positioned at least partially within the at least one through bore of the shell such that, in an assembled state, the shell and the at least one augment define a modified external shape.

Abstract: A prosthesis according to the present disclosure includes a shell. A liner is disposed within the shell, and a femoral head may be disposed within the liner. A locking mechanism may assist in securing the liner within the shell. The locking mechanism may be removed when the shell, liner, and femoral head are implanted. The shell extends beyond a hemisphere of the shell, and the liner extends beyond a hemisphere of the liner.

Abstract: Disclosed is an orthopedic implant that includes an anchor, a bore, and a compressible and expandable mesh. The anchor is configured to secure the implant at an implantation site and defines a longitudinal axis. The bore is defined by the anchor and extends along the longitudinal axis. The compressible and expandable mesh is aligned along the longitudinal axis and defines a plurality of openings. The mesh is configured to compress along the longitudinal axis and expand from the longitudinal axis to engage surrounding bone or tissue at the implantation site to secure the implant at the implantation site.

Abstract: According to various embodiments, a trial system (100) and instruments can be used to assist in confirming that a planned procedure is achieved. In various embodiments, the trial or provisional portions can include markings (110) on a trial or provisional portion to compare to one or more implanted members to ensure an planned position is achieved.

Abstract: Disclosed is an orthopedic implant that includes an anchor, a bore, and a compressible and expandable mesh. The anchor is configured to secure the implant at an implantation site and defines a longitudinal axis. The bore is defined by the anchor and extends along the longitudinal axis. The compressible and expandable mesh is aligned along the longitudinal axis and defines a plurality of openings. The mesh is configured to compress along the longitudinal axis and expand from the longitudinal axis to engage surrounding bone or tissue at the implantation site to secure the implant at the implantation site.

Abstract: Disclosed is a modular trial system to select a neck length. The system may be in a hexagonal or click embodiments. A neck member may having at least a locating step with a locating step face. A head member may have at least a first groove and a second groove in an internal bore. The head member may be rotated relative to the neck member to select various trial lengths of the neck.

Abstract: A prosthesis can have a wall portion that deforms to conform to a surface. The deformation of the wall can be plastic (i.e. permanent) or elastic (i.e. able to return to the pre-deformed configuration). The surface can be an anatomical surface.