Cortina [MAX] Lumbar Cage System

Cortina [MAX] Lumbar Cage System is an FDA 510(k)-cleared medical device (K180431) manufactured by Neurostructures, 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 March 21, 2018. Regulation: 8.