Altus Spine Interbody Standalone Fusion System

Altus Spine Interbody Standalone Fusion System is an FDA 510(k)-cleared medical device (K211837) manufactured by Altus Partners, 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 April 18, 2022. Regulation: 8.