Nextra CH Cannulated Hammertoe System

Nextra CH Cannulated Hammertoe System is an FDA 510(k)-cleared medical device (K213530) 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 December 8, 2021. Regulation: 8.