SYNTHES ELASTIC INTRAMEDULLARY NAIL (EIN) SYSTEM

SYNTHES ELASTIC INTRAMEDULLARY NAIL (EIN) SYSTEM is an FDA 510(k)-cleared medical device (K971783) manufactured by Synthes (Usa). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 17, 1997. Regulation: 8.