Genesys Spine Sacroiliac Joint Fusion System with Navigation

Genesys Spine Sacroiliac Joint Fusion System with Navigation is an FDA 510(k)-cleared medical device (K233595) manufactured by Genesys Spine. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 28, 2024. Regulation: 8.