SAGITTAL & ROTARY ACT/PASS KNEE LIGAMENT TESTER

SAGITTAL & ROTARY ACT/PASS KNEE LIGAMENT TESTER is an FDA 510(k)-cleared medical device (K861622) manufactured by Orthopedic Systems, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 26, 1986. Regulation: 8.