IdentiTi Porous Ti Interbody System

IdentiTi Porous Ti Interbody System is an FDA 510(k)-cleared medical device (K183705) manufactured by Alphatec Spine, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 2019. Regulation: 8.