Keos Anterior Cervical Interbody Fusion Device System

Keos Anterior Cervical Interbody Fusion Device System is an FDA 510(k)-cleared medical device (K212450) manufactured by Keos. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 5, 2022. Regulation: 8.