AccuLIF TL and PL Cage

AccuLIF TL and PL Cage is an FDA 510(k)-cleared medical device (K160715) manufactured by Stryker Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 7, 2016. Regulation: 8.