STRYKER UNIVERSAL ACL INSTRUMENTATION SYSTEM

STRYKER UNIVERSAL ACL INSTRUMENTATION SYSTEM is an FDA 510(k)-cleared medical device (K951267) manufactured by Stryker Endoscopy. 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 31, 1995. Regulation: 8.