Camber Sacroiliac (SI) Fixation System

Camber Sacroiliac (SI) Fixation System is an FDA 510(k)-cleared medical device (K233972) 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 February 26, 2024. Regulation: 8.