Spineart gains FDA clearance for anterior cervical cage

Spineart received FDA 510(k) clearance for its SCARLET AC-Ti secured anterior cervical cage.

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The SCARLET AC-Ti uses Spineart’s proprietary Ti-LIFE technology, an additive manufacturing process that has a porous structure that mimics the trabecular bone structure, according to a May 28 news release from Spineart.

The SCARLET AC-Ti is part of the SCARLET system.

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