CD LIBERTY POSTERIOR SPINCAL SYSTEM

CD LIBERTY POSTERIOR SPINCAL SYSTEM is an FDA 510(k)-cleared medical device (K951164) manufactured by Sofamor Danek USA,Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 8, 1996. Regulation: 8.