Alphatec Solus Fusion Device Receives FDA 510(k) Clearance

Spinal Tech

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