Spinal Intervertebral Body Fixation Orthosis
- UID
- IMP/MD/2021/000329_a81da6ec3e559b36f0ec0077a1a5a7be_adedbb1f8f25829dff3790f35bb9e019
- Device class
- Class D
- Brand name
- C7 Cage
- License holder
- MEDYSSEY INDIA PRIVATE LIMITED
- Approving authority
- CDSCO
- Product information
- The LP Cage is indicated for use with autogenous bone graft patients with degenerative disc disease and this LP Cage is designed to utilizing the management on the degenerative disc disease of the extensive spinal column, from thoracic to sacral spine, include isolated disc resorption, primary and secondary instability, recurrent disc herniation, and pseudarthosis. The LP Cage is an interbody fusion cage of implants and instruments designed for posterior lumbar interbody fusion(C7 Cage). This LP Cage must be used with Spinal supplemental fixation for stability. There are general symptoms of intended use which in Indications. They are indicated for: Primary surgery for advanced discopathies or extensive decompressions (C7 Cage) Spondylotic spinal stenosis Revision surgery for failed disc operation Post-operative instability Disc herniation Spondylosis with bone spurring, foraminal narrowing and nerve root impingenment Chronic and disabling discogenic low back pain Spinal pseudarthrosis
Spinal Intervertebral Body Fixation Orthosis is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000329_a81da6ec3e559b36f0ec0077a1a5a7be_adedbb1f8f25829dff3790f35bb9e019. This device is marketed under the brand name C7 Cage. The license holder is MEDYSSEY INDIA PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is CDSCO.
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