Curiteva Anterior Cervical Plate System

Curiteva Anterior Cervical Plate System is an FDA 510(k)-cleared medical device (K181562) manufactured by Curiteva, 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 1, 2018. Regulation: 8.