Singapore - English - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - duraloc constrained acetabular liner system is intended to use as components of a total hip prosthesis 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.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 38156 - ceramic femoral head prosthesis - a biolox delta ts ceramic femoral head is composed of a packaged biolox delta ceramic femoral head with metal tapered sleeve adapters. the biolox delta ts ceramic femoral head is manufactured from biolox delta alumina matrix composite ceramic. the biolox delta ts ceramic head is intended to allow assembly with depuy femoral hip stem tapers, either in a primary hip replacement surgery, or in revision hip replacement surgery with well-fixed femoral stems. the depuy delta taper sleeve (ts) ceramic femoral head is intended for use in total hip arthroplasty applications to replace the articular surface of the femoral head in primary hip surgery and for the salvage of a failed previous hip surgery. total hip arthroplasty 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.

Singapore - English - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - depuy marathon xlpe cemented cup is indicated for joint replacement, for severe arthropathy due to advanced rheumatoid or osteo-arthritis where conservative therapy or alternative treatments have failed or are considered unsuitable, arthropathy due to degenerative disease, acute trauma, and a previous failed joint replacement. the patient’s joint must be anatomically and structurally suited to receive the selected implant(s).

Singapore - English - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - when used with compatible femoral components, the knee system is indicated for cemented use in cases of osteoarthritis and rheumatoid arthritis. the porous coated keeled and non keeled m.b.t.™ (mobile bearing tibial) tray configurations of the lcs total knee system are indicated for noncemented use in skeletally mature individuals undergoing primary surgery for reconstructing knees damaged as a result of noninflammatory degenerative joint disease (nidjd) or either of its composite diagnoses of osteoarthritis and post-traumatic arthritis pathologies. the rotating platform device configuration is indicated for use in knees whose anterior and posterior cruciate ligaments are absent or are in such condition as to justify their sacrifice. the p.f.c. sigma rp curved bearings when used with the p.f.c. sigma cruciate retaining femoral component can be used in posterior cruciate ligament retaining procedures.

Singapore - English - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - are intended to be used for hemi-hip arthroplasty where there is evidence of a satisfactory natural acetabulum and sufficient femoral bone to seat and support the femoral stem.

Singapore - English - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - total hip arthroplasty 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. a vascular 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. porous-coated pinnacle acetabular cups are indicated for cementless application.

Singapore - English - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - the depuy pinnacle acetabular cup system is indicated for use in total hip replacement procedures. total hip arthroplasty 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 all pinnacle porous-coated acetabular shells are indicated for cementless application.

Singapore - English - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - total hip arthroplasty 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 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.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 35217 - cement, orthopaedic, bone - indicated for the use of fixation of prosthesis to living bone arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk. the bone cement should be used with an appropriate prosthesis. indicated for the use of fixation of prosthesis to living bone arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk. the bone cement should be used with an appropriate prosthesis.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 35217 - cement, orthopaedic, bone - indicated for the use of fixation of prosthesis to living bone arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk. the bone cement should be used with an appropriate prosthesis. indicated for the use of fixation of prosthesis to living bone arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk. the bone cement should be used with an appropriate prosthesis.