
Cook Biotech, Inc.
Free shipping on orders over $99 · 30-day returns
DURASIS DURAL SUBSTITUTE is an FDA 510(k)-cleared medical device (K031850) manufactured by Cook Biotech, 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 September 7, 2003. Regulation: 8.