Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - when used as a pedicle screw fixation system, it is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the posterior thoracic, lumbar, and sacral spine: degenerative disc disease, degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor and/or failed previous fusion (pseudoarthrosis). it is also indicated for the treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebral joint in skeletally mature patients receiving fusion by autogenous bone graft, having the device fixed or attached to the lumbar and sacral spine (l3 to sacrum), with removal of the implants after attainment of a solid fusion. when used as an anterolateral non-pedicle screw system in the thoracic and lumbar spine,it is also intended for: degenerative disc disease, spinal stenosis, spondyl

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - pedicle screw fixation: immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of degenerative disc disease, degenerative spondylolisthesis, fracture, dislocation, scoliosis, kyphosis, spinal tumour and/or pseudoarthrosis posterior non-cervical screw fixation in pediatric patients: adjunct to fusion to treat idiopathic scoliosis; those diagnosed with spondylolisthesis/spondylolysis; fracture caused by tumour and/or trauma treatment of severe spondylolisthesis of l5-s1 vertebral joint in skeletally mature patients receiving fusion by autogenous bone graft, with device fixed or attached to the lumbar and sacral spine (l3 to sacrum), with removal of the implants after attainment of a solid fusion. anterolateral non-pedicle screw system: degenerative disc disease, spinal stenosis, spinal deformities, fractures, spondylolisthesis, spinal deformities, fracture, pseudoarthrosis, tumor resection, and/or failed previous fusion

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - when used as a pedicle screw fixation system, it is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the posterior thoracic, lumbar, and sacral spine: degenerative disc disease, degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor and/or failed previous fusion (pseudoarthrosis). it is also indicated for the treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebral joint in skeletally mature patients receiving fusion by autogenous bone graft, having the device fixed or attached to the lumbar and sacral spine (l3 to sacrum), with removal of the implants after attainment of a solid fusion. when used as an anterolateral non-pedicle screw system in the thoracic and lumbar spine, it is also intended for: degenerative disc disease, spinal stenosis

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - when used as a pedicle screw fixation system, it is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the posterior thoracic, lumbar, and sacral spine: degenerative disc disease, degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor and/or failed previous fusion (pseudoarthrosis). it is also indicated for the treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebral joint in skeletally mature patients receiving fusion by autogenous bone graft, having the device fixed or attached to the lumbar and sacral spine (l3 to sacrum), with removal of the implants after attainment of a solid fusion. when used as an anterolateral non-pedicle screw system in the thoracic and lumbar spine, it is also intended for: degenerative disc disease, spinal stenosis

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - when used as a pedicle screw fixation system, it is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the posterior thoracic, lumbar, and sacral spine: degenerative disc disease, degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor and/or failed previous fusion (pseudoarthrosis). it is also indicated for the treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebral joint in skeletally mature patients receiving fusion by autogenous bone graft, having the device fixed or attached to the lumbar and sacral spine (l3 to sacrum), with removal of the implants after attainment of a solid fusion. when used as an anterolateral non-pedicle screw system in the thoracic and lumbar spine, it is also intended for: degenerative disc disease, spinal stenosis,

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - when used as a pedicle screw fixation system, it is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the posterior thoracic, lumbar, and sacral spine: degenerative disc disease, degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor and/or failed previous fusion (pseudoarthrosis). it is also indicated for the treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebral joint in skeletally mature patients receiving fusion by autogenous bone graft, having the device fixed or attached to the lumbar and sacral spine (l3 to sacrum), with removal of the implants after attainment of a solid fusion. when used as an anterolateral non-pedicle screw system in the thoracic and lumbar spine, it is also intended for: degenerative disc disease, spinal stenosis

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - is indicated for use via the lateral or anterolateral surgical approach above the bifurcation of the great vessels in the treatment of thoracic and thoracolumbar (t1-l5) spine instability or via the anterior surgical approach, below the bifurcation of the great vessels, in the treatment of lumbar and lumbosacral (l1-s1) spine instability as a result of: 1. fracture (including dislocation and subluxation) 2. tumor 3. degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies) 4. scoliosis 5. kyphosis 6. lordosis 7. spinal stenosis 8. failed previous spine surgery

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - is intended to promote fusion of the cervical spine and occipito-thoracic junction (occiput-t3). the vuepoint® oct system is indicated for: 1. degenerative disc disease (as defined by back pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies); 2. degenerative spondylolisthesis with objective evidence of neurologic impairment; 3. fracture/dislocation; 4. spinal stenosis; 5. atlantoaxial fracture with instability; 6. occipitocervical dislocation; 7. spinal tumor and/or; 8. revision of previous cervical spine surgery; the occipital bone screws are limited to occipital fixation only. the use of polyaxial screws is limited to placement in the upper thoracic spine (t1-t3) in treating thoracic conditions only. they are not intended to be placed in the cervical spine.

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - the armada rods when used with the compatible constituent components as a pedicle screw fixation system, is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the posterior thoracic, lumbar, and sacral spine. indications: 1. degenerative disc disease 2. degenerative spondylolisthesis with objective evidence of neurologic impairment 3. fracture 4. dislocation 5. scoliosis 6. kyphosis 7. spinal tumor and/or 8. failed previous fusion (pseudoarthrosis). it is also indicated for the treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebral joint in skeletally mature patients receiving fusion by autogenous bone graft, having the device fixed or attached to the lumbar and sacral spine (l3 to sacrum), with removal of the implants after attainment of a solid fusion. the rods when used with the compatible constituent components as an anterol

Singapore - inglese - HSA (Health Sciences Authority)

nuvasive southeast asia pte. ltd. - orthopaedics - when used as a pedicle screw fixation system, it is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the posterior thoracic, lumbar, and sacral spine: degenerative disc disease, degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor and/or failed previous fusion (pseudoarthrosis). it is also indicated for the treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebral joint in skeletally mature patients receiving fusion by autogenous bone graft, having the device fixed or attached to the lumbar and sacral spine (l3 to sacrum), with removal of the implants after attainment of a solid fusion. when used as an anterolateral non-pedicle screw system in the thoracic and lumbar spine, it is also intended for: degenerative disc disease, spinal stenosis