KAPHORN
KAPHORN is a side loading posterior osteosynthesis system.
It is intended for the reduction of pathologies of the thoraco-lombo-sacral spine by restoring the disc height as well as the physiological bending of the spine
Implant material: titanium alloy T6AV (ISO 5832-3 and ASTM F136).
Instrument material : stainless steel (EN 10088-2, EN 10216-5, ASTM A213), titanium (5832-3 or 5832-2), polymers
KAPHORN system can be used in skeletally mature individuals (adults) and in adolescent population for specific indications such as scoliosis.
This medical device is intended for the posterior fixation of the thoracic, lumbar and sacral spine. It is indicated for the treatment of
- deformities (any etiology)
- Trauma
- Tumors
- the degenerative spine (spondylolisthesis, degenerative disc disease, spinal fractures, spinal stenosis, non-union)
KAPHORN can also be used in revision surgery in case of failure of a previous procedure.
KAPHORN is CE marked and approved for use in Europe. It is not approved by FDA for use in the US.
OPEN THORACOLUMBAR ARTHRODESIS
mont blanc 3D+
Coplanar Alignment System
VEOS PEEK
Flexible Posterior Osteosynthesis System