FDA Grants 510(k) Clearance to Alphatec Solus Fusion Device

The FDA granted 510(k) clearance to Alphatec Spine’s Alphatec Solus internal fixation anterior lumbar interbody fusion device.

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The ALIF device includes counter-rotating titanium blades that deploy into adjacent vertebrae and lock the device in place, according to the release. Alphatec launched the device in Europe last month.

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