RIGEL PEEK Anterior Cervical Interbody Fusion System

RIGEL PEEK Anterior Cervical Interbody Fusion System is an FDA 510(k)-cleared medical device (K190618) manufactured by MiRus, 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 June 5, 2019. Regulation: 8.