Amedica Valeo II Interbody Fusion Device

Amedica Valeo II Interbody Fusion Device is an FDA 510(k)-cleared medical device (K142347) 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 November 17, 2014. Regulation: 8.