Luna XD Ti Interbody Fusion System

Luna XD Ti Interbody Fusion System is an FDA 510(k)-cleared medical device (K193172) manufactured by Benvenue Medical, 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 July 1, 2020. Regulation: 8.