Valeo® C+CSC with Lumen Interbody Fusion Device

Valeo® C+CSC with Lumen Interbody Fusion Device is an FDA 510(k)-cleared medical device (K173453) 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 March 4, 2018. Regulation: 8.