Hammerdesis™ Interphalangeal Fusion System

Hammerdesis™ Interphalangeal Fusion System is an FDA 510(k)-cleared medical device (K231147) manufactured by Intelivation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 2023. Regulation: 8.