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Spinal Intervertebral Body Fixation Orthosis - India CDSCO Medical Device Registration

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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CDSCO Registered
Class Class D
Spinal Intervertebral Body Fixation Orthosis
UID: IMP/MD/2021/000329_a81da6ec3e559b36f0ec0077a1a5a7be_adedbb1f8f25829dff3790f35bb9e019

Brand Name

C7 Cage

Device Class

Class D

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

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