DuoHex CH Cannulated Hammertoe System

DuoHex CH Cannulated Hammertoe System is an FDA 510(k)-cleared medical device (K200840) manufactured by Nextremity Solutions, 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 June 25, 2020. Regulation: 8.