KINEMATIC KNEE DEVICE/MAGNETOM OPEN SYSTEM

KINEMATIC KNEE DEVICE/MAGNETOM OPEN SYSTEM is an FDA 510(k)-cleared medical device (K961121) manufactured by Siemens Medical Solutions USA, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 18, 1996. Regulation: 8.