Altus Spine Titanium Interbody Fusion System

Altus Spine Titanium Interbody Fusion System is an FDA 510(k)-cleared medical device (K171329) 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 August 28, 2017. Regulation: 8.