Curiteva Porous PEEK Laminoplasty System

Curiteva Porous PEEK Laminoplasty System is an FDA 510(k)-cleared medical device (K243137) 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 October 27, 2024. Regulation: 8.