Acro Composites Interbody System

Acro Composites Interbody System is an FDA 510(k)-cleared medical device (K230478) manufactured by Acro Composites, LLC. 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 18, 2023. Regulation: 8.