Siconus SI Joint Fixation System

Siconus SI Joint Fixation System is an FDA 510(k)-cleared medical device (K162121) manufactured by Camber Spine Technologies. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 17, 2017. Regulation: 8.