MEDTRONIC MODEL 3530 PERCUTANEOUS EXTENSION

MEDTRONIC MODEL 3530 PERCUTANEOUS EXTENSION is an FDA 510(k)-cleared medical device (K892884) manufactured by Medtronic Vascular. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 6, 1989. Regulation: 8.