Pinnacle 300 Acetabular Shell with Porocoat - Acetabular shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle 300 acetabular shell with porocoat - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle 300 acetabular shell with porocoat are titanium shells coated in porocoat (titanium sintered beads) to enable biological fixation into the prepared acetabulum. three coated spikes located on the radius support for additional fixation. an appropriate liner is then placed into the implanted shell. the pinnacle 300 acetabular shell with porocoat is an acetabular shell used during primary or revision total hip arthroplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis. the pinnacle 300 acetabular shell with porocoat is indicated for cementless applications.

Pinnacle 100 Acetabular Shell with Gription - Acetabular shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle 100 acetabular shell with gription - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle 100 acetabular shells with gription are titanium shells coated in gription to enable biological, cementless fixation into the prepared acetabulum. an appropriate liner is placed into the shell. the pinnacle 100 acetabular shell with gription is the acetabular shell component used during primary or revision total hip arthroplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis.

Pinnacle Constrained Acetabular Liner - Constrained polyethylene acetabular liner Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle constrained acetabular liner - constrained polyethylene acetabular liner

johnson & johnson medical pty ltd t/a depuy synthes - 44362 - constrained polyethylene acetabular liner - the pinnacle constrained acetabular liner is manufactured from cross-linked uhmwpe, which locks into an outer shell component. the liner component articulates with a metal femoral head of an appropriate diameter. the pinnacle constrained acetabular liner mechanically constrains the femoral head within the inner diameter of the liner with a titanium constraining ring which fits over the opening diameter of the liner. the uhmwpe liner is held in the metal shell by means of a titanium locking ring. the pinnacle constrained acetabular liner is indicated for use as a component of a total hip prosthesis in primary or revision patients at high risk of hip dislocation due to a history of prior dislocation, bone loss, joint or soft tissue laxity, neuromuscular disease or intraoperative instability. the pinnacle constrained acetabular liner is indicated for use with the pinnacle acetabular cup in cementless application.

Pinnacle Revision Acetabular Shell with Gription - Acetabular shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle revision acetabular shell with gription - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle revision acetabular shells with gription are titanium shells coated in gription (titanium sintered particles on a titanium sintered beads substrate) to enable biological fixation into the prepared acetabulum. the pinnacle revision acetabular shells with gription is intended for cementless applications and includes additional peripheral screw holes. an appropriate liner is then placed into the implanted shell. the pinnacle revision acetabular shell with gription is used in cases of revision of total hip arthroplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis.

Pinnacle 100 Acetabular Shell with Porocoat - Acetabular shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle 100 acetabular shell with porocoat - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle acetabular 100 shells with porocoat are titanium shells coated in porocoat (titanium sintered beads) to enable biological fixation into the prepared acetabulum. an appropriate liner is then placed into the implanted shell. the pinnacle 100 acetabular shell with porocoat is an acetabular shell used during primary or revision total hip arthroplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis.

Pinnacle 100 Acetabular Shell with Duofix - Acetabular shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle 100 acetabular shell with duofix - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle 100 acetabular shells with duofix are titanium shells coated in duofix (combination of sintered titanium metal beads and hydroxyapatite) to enable biological fixation into the prepared acetabulum. an appropriate liner is then placed into the implanted shell. the pinnacle 100 acetabular shell with duofix is an acetabular shell used during primary or revision total hip arthoplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis.

Pinnacle Sector Acetabular Shell with Duofix - Acetabular shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle sector acetabular shell with duofix - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle sector acetabular shells with duofix are titanium shells coated in duofix (combination of sintered titanium metal beads and hydroxyapatite) to enable biological fixation into the prepared acetabulum. these shells are indicated for cementless applications. additionally, the pinnacle sector acetabular shells with duofix have three screw holes for optional adjunct fixation and access to the ilium and posterior column. an appropriate liner is then placed into the implanted shell. the pinnacle sector acetabular shell with duofix is an acetabular shell used during primary or revision total hip arthroplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis.

Pinnacle Acetabular Shell with Porocoat - Acetabular shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle acetabular shell with porocoat - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle acetabular shells with porocoat are titanium shells coated in porocoat (titanium sintered beads) to enable biological fixation into the prepared acetabulum. pinnacle acetabular shells with porocoat are indicated for cementless applications. additionally, the pinnacle acetabular shells with porocoat are available with of a range of holes to enable screws. an appropriate liner is then placed into the implanted shell. the pinnacle acetabular shell with porocoat is an acetabular shell used during primary or revision total hip arthroplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis.

Pinnacle Acetabular Shells with Gription - Acetabular Shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle acetabular shells with gription - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle acetabular shells with gription are titanium shells coated in gription (titanium sintered particles on a titanium sintered beads substrate) to enable cementless, biological fixation into the prepared acetabulum. additionally, the pinnacle acetabular shells with gription are available with of a range of holes to allow screws. an appropriate liner is then placed into the implanted shell. the pinnacle acetabular shell with gription is the acetabular shell component used during primary or revision total hip arthroplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis.

Pinnacle Deep Profile Revision Acetabular Shell with Gription - Acetabular shell Australia - English - Department of Health (Therapeutic Goods Administration)

pinnacle deep profile revision acetabular shell with gription - acetabular shell

johnson & johnson medical pty ltd t/a depuy synthes - 43167 - acetabular shell - the pinnacle deep profile revision acetabular shells with gription are titanium shells coated in gription (titanium sintered particles on a titanium sintered beads substrate) to enable biological (cementless) fixation into the prepared acetabulum. an appropriate liner is then placed into the implanted shell. the deep profile option allows the surgeon to address soft tissue laxity. the device has dome holes and 8 peripheral screw holes. the pinnacle deep profile revision acetabular shell with gription is used in cases of revision of total hip arthroplasty and is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis.