ECTRA LIGAMENT RELEASE SYSTEM

ECTRA LIGAMENT RELEASE SYSTEM is an FDA 510(k)-cleared medical device (K953387) manufactured by Smith & Nephew Dyonics, 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 August 8, 1995. Regulation: 8.