THE NAVIGATOR STEERABLE GUIDE WIRE

THE NAVIGATOR STEERABLE GUIDE WIRE is an FDA 510(k)-cleared medical device (K860430) manufactured by Meadox Surgimed, 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 July 17, 1986. Regulation: 8.