Oculus-SA Lumbar Cage System

Oculus-SA Lumbar Cage System is an FDA 510(k)-cleared medical device (K202190) manufactured by Neurostructures. 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 1, 2020. Regulation: 8.