IdentiTi™ II Interbody System

IdentiTi™ II Interbody System is an FDA 510(k)-cleared medical device (K242364) 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 October 3, 2024. Regulation: 8.