CORDIS POLYPROPYLENE BURR HOLE RESERVOIR

CORDIS POLYPROPYLENE BURR HOLE RESERVOIR is an FDA 510(k)-cleared medical device (K925810) manufactured by Cordis Corp.. 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 1, 1994. Regulation: 8.