Alphatec Holdings has received 510(k) clearance from the FDA for its Solus Anterior Lumbar Interbody Fusion system, according to a company news release.
The Solus ALIF device, which is now available for commercial release in the U.S., features an integrated fixation method based on intellectual property previously acquired by the company. The patented fixation technology allows for enhanced segmental stability with a simplified surgical technique, while providing for substantial spacing to add bone graft.
Read the company news release about Alphatec Spine's Solus ALIF device.
Read other coverage about Alphatec Spine:
- Alphatec Spine Receives CE Mark of Approval for Spinal Systems
- Alphatec Spine Reports 4Q Revenue of $46M, 38.4% Increase
- DJO Global CEO Leslie Cross Joins Alphatec Spine's Board of Directors
The Solus ALIF device, which is now available for commercial release in the U.S., features an integrated fixation method based on intellectual property previously acquired by the company. The patented fixation technology allows for enhanced segmental stability with a simplified surgical technique, while providing for substantial spacing to add bone graft.
Read the company news release about Alphatec Spine's Solus ALIF device.
Read other coverage about Alphatec Spine:
- Alphatec Spine Receives CE Mark of Approval for Spinal Systems
- Alphatec Spine Reports 4Q Revenue of $46M, 38.4% Increase
- DJO Global CEO Leslie Cross Joins Alphatec Spine's Board of Directors