Curiteva Sacroiliac Joint Fusion System

Curiteva Sacroiliac Joint Fusion System is an FDA 510(k)-cleared medical device (K210402) 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 September 8, 2021. Regulation: 8.