Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System)

Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System) is an FDA 510(k)-cleared medical device (K181549) 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 2, 2018. Regulation: 8.