NITRO Interbody Fusion Cage System Family

NITRO Interbody Fusion Cage System Family is an FDA 510(k)-cleared medical device (K220513) manufactured by Ctl Medical 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 April 24, 2023. Regulation: 8.