Tritanium® TL Curved Posterior Lumbar Cage

Tritanium® TL Curved Posterior Lumbar Cage is an FDA 510(k)-cleared medical device (K173476) manufactured by Stryker. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 17, 2018. Regulation: 8.