VISIONSENSE STEREOSCOPIC VISION SYSTEM

VISIONSENSE STEREOSCOPIC VISION SYSTEM is an FDA 510(k)-cleared medical device (K082355) manufactured by Visionsense, Ltd.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 14, 2008. Regulation: 8.