ENDOSCOPIC MORTONS NEUROMA INSTRUMENTS

ENDOSCOPIC MORTONS NEUROMA INSTRUMENTS is an FDA 510(k)-cleared medical device (K940230) manufactured by Instratek, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 11, 1994. Regulation: 8.