Depuy Attune Revision Knee System Singapore - English - HSA (Health Sciences Authority)

depuy attune revision knee system

johnson & johnson international (singapore) pte ltd - orthopaedics - intended for total knee arthroplasty, designed to provide increased patient mobility and reduced pain by replacing damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat & support the components. attune revision rotating platform knee system is indicated for cemented use in cases of osteoarthritis & rheumatoid arthritis. the rotating platform prosthesis is indicated for primary total knee arthroplasty or revision of failed knee prostheses. attune revision knee system fixed bearing system is designed for use in total knee arthroplasty for patients with: • absence or loss of both cruciate ligaments • moderate varus-valgus or flexion instability that requires a bearing surface with increased constraint in the clinical judgment of the surgeon • bone loss that requires supplemental fixation in the clinical judgment of the surgeon the porous-coated metaphyseal sleeves are intended for either cemented or cementless applications

DePuy ATTUNE Total Knee System Singapore - English - HSA (Health Sciences Authority)

depuy attune total knee system

johnson & johnson international (singapore) pte ltd - orthopaedics - intended for cemented and cementless use as a total knee replacement system. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post traumatic arthritis, rheumatoid arthritis, or a failed previous implant. attune® revision knee implants are designed for use in total knee arthroplasty for patients with: • absence or loss of both cruciate ligaments • moderate varus-valgus or flexion instability that requires a bearing surface with increased constraint in the clinical judgment of the surgeon • bone loss that requires supplemental fixation in the clinical judgment of the surgeon.

DePuy C-STEM™ AMT Hip System Singapore - English - HSA (Health Sciences Authority)

depuy c-stem™ amt hip system

johnson & johnson international (singapore) pte ltd - orthopaedics - total hip arthroplasty is intended to replace the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. hemi-hip protheses replaces the damaged hip joint articulation in patients where there is evidence of a satisfactory natural acetabulum and sufficient bone seat and support the femoral stem. total hip replacement is indicated in the following conditions: 1. a severely painful and/or arthritic joint (typically due to non-inflammatory degenerative joint disease) 2. failed previous hip surgery 3. acute fracture of the femoral head or neck hemi hip replacement is indicated in the following conditions: 1. acute fracture of the femoral head or neck.

Depuy Cement Restrictor Singapore - English - HSA (Health Sciences Authority)

depuy cement restrictor

johnson & johnson international (singapore) pte ltd - orthopaedics - the uhmwpe cement restrictor is intended for use in cemented total and hemiarthroplasty procedures to restrict distal flow of bone cement in the femoral medullary cavity.

DePuy Cervical IF Cage Singapore - English - HSA (Health Sciences Authority)

depuy cervical if cage

johnson & johnson international (singapore) pte ltd - orthopaedics - is indicated for treatment for the following conditions: 1. interbody fusion for recurrent or residual back, leg or neck pain following discectomy. 2. interbody fusion for disabling back or neck pain in the presence of objective instability and/or spondylolisthesis. 3. multiple level interbody fusion for treatment of multiple level discogenic disease. 4. interbody fusion for previous failed surgery or failed fusion. 5. vertebral body replacement for tumor or trauma.

Depuy Concorde™ VBR Spinal System Singapore - English - HSA (Health Sciences Authority)

depuy concorde™ vbr spinal system

johnson & johnson international (singapore) pte ltd - orthopaedics - indicated for use in the thoracolumbar spine (i.e., t1 to l5) to replace a diseased vertebral body resected or excised for the treatment of tumors, to achieve anterior decompression of the spinal cord and neural tissues, and to restore the height of a collapsed vertebral body. the vbr spinal systems are also indicated for treating fractures of the thoracic and lumbar spine. the vbr spinal systems are designed to restore the biomechanical integrity of the anterior, middle and posterior spinal column even in the absence of fusion for a prolonged period. the vbr spinal systems are intended for use with supplemental internal fixation. the supplemental internal fixation systems that may be used include titanium plate or rod systems.

DePuy Corail Hip System - Cemented Femoral Stems Singapore - English - HSA (Health Sciences Authority)

depuy corail hip system - cemented femoral stems

johnson & johnson international (singapore) pte ltd - orthopaedics - the hip prosthesis is intended for use in total hip arthroplasty 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, superficial replacement arthroplasty or total hip replacement. 5. certain cases of ankylosis.

DePuy Corail™ AMT Hip Prosthesis System Singapore - English - HSA (Health Sciences Authority)

depuy corail™ amt hip prosthesis system

johnson & johnson international (singapore) pte ltd - orthopaedics - the corail amt hip prosthesis is intended for use in total and partial hip arthroplasty (corail amt stem size 6 is indicated for total hip arthroplasty only). the stems are intended only for uncemented use. 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. partial hip arthroplasty (hip hemiarthroplasty) is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of a satisfactory natural acetabulum and sufficient femoral bone to seat and support the femoral stem.

DePuy Delta Xtend™ Reverse Shoulder System Singapore - English - HSA (Health Sciences Authority)

depuy delta xtend™ reverse shoulder system

johnson & johnson international (singapore) pte ltd - orthopaedics - the delta xtend prosthesis is indicated for use in treatment of a grossly deficient rotator cuff joint with: -severe arthropathy and/or; -a previous failed joint replacement and/or; -fracture-dislocations, of the proximal humerus where the articular surface is severely communited, separated from its blood supply or where the surgeon’s experience indicates that alternative methods of treatment are unsatisfactory the patient’s joint must be anatomically and structurally suited to receive the selected implant(s), and a functional deltoid muscle is necessary to use the device. delta xtend hemi-shoulder replacement is also indicated for hemi-arthroplasty if the glenoid is fractured intraoperatively or for the revision of a previously failed delta xtend reverse shoulder.

DePuy Expedium™ Spine System - Titanium Singapore - English - HSA (Health Sciences Authority)

depuy expedium™ spine system - titanium

johnson & johnson international (singapore) pte ltd - orthopaedics - intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine. intended for noncervical pedicle fixation and nonpedicle fixation for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e. fracture or dislocation); spinal stenosis; curvatures (i.e. scoliosis, kyphosis, and/or lordosis); tumor; pseudoarthrosis; and failed previous fusion in skeletally mature patients. peek rods are contraindicated for degenerative disc disease.