Curiteva Laminoplasty System

Curiteva Laminoplasty System is an FDA 510(k)-cleared medical device (K231232) manufactured by Curiteva, Inc.. 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 27, 2023. Regulation: 8.