CODMAN ETHISORB DURA PATCH

CODMAN ETHISORB DURA PATCH is an FDA 510(k)-cleared medical device (K991413) manufactured by Johnson & Johnson Professionals, 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 March 12, 2000. Regulation: 8.