Advantage-C PEEK Cervical lnterbody Fusion Device

Advantage-C PEEK Cervical lnterbody Fusion Device is an FDA 510(k)-cleared medical device (K211501) manufactured by Lntelivation, 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 August 23, 2021. Regulation: 8.