MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE

MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE is an FDA 510(k)-cleared medical device (K925342) manufactured by Medtronics Interventional Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 5, 1993. Regulation: 8.