Triton™ Sacroiliac Joint Fixation System

Triton™ Sacroiliac Joint Fixation System is an FDA 510(k)-cleared medical device (K211449) manufactured by Choice Spine, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 30, 2021. Regulation: 8.