Valeo II Interbody Fusion Device System

Valeo II Interbody Fusion Device System is an FDA 510(k)-cleared medical device (K161405) manufactured by Amedica Corp.. 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 18, 2016. Regulation: 8.