AGILITY STEERABLE GUIDEWIRE NEUROSCOUT STEERABLE GUDIEWIRE

AGILITY STEERABLE GUIDEWIRE NEUROSCOUT STEERABLE GUDIEWIRE is an FDA 510(k)-cleared medical device (K121776) manufactured by Codman & Shurtleff, 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 August 13, 2012. Regulation: 8.