AGILITY STEERABLE GUIDEWIRE

AGILITY STEERABLE GUIDEWIRE is an FDA 510(k)-cleared medical device (K001033) manufactured by Cordis Neurovascular, 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 April 13, 2000. Regulation: 8.