MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002

MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002 is an FDA 510(k)-cleared medical device (K903018) manufactured by Medtronic Andover Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 2, 1990. Regulation: 8.