Curiteva Thoracolumbar Plate System

Curiteva Thoracolumbar Plate System is an FDA 510(k)-cleared medical device (K233360) 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 February 28, 2024. Regulation: 8.