Centinel Spine STALIF TT, STALIF MIDLINE, MIDLINE II, MIDLINE II-Ti

Centinel Spine STALIF TT, STALIF MIDLINE, MIDLINE II, MIDLINE II-Ti is an FDA 510(k)-cleared medical device (K150643) manufactured by Centinel 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 June 7, 2015. Regulation: 8.