CODMAN DURAFORM DURAL GRAFT IMPLANT

CODMAN DURAFORM DURAL GRAFT IMPLANT is an FDA 510(k)-cleared medical device (K041518) manufactured by Codman & Shurtleff, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 21, 2004. Regulation: 8.