DePuy Synthes Hammertoe Continuous Compression Implant

DePuy Synthes Hammertoe Continuous Compression Implant is an FDA 510(k)-cleared medical device (K191463) manufactured by Synthes (USA) Products, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 25, 2020. Regulation: 8.