Alphatec Spine Receives 510(k) Clearance for Solus System

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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.

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