NK DEVIATION SENSOR, MODEL DV001

NK DEVIATION SENSOR, MODEL DV001 is an FDA 510(k)-cleared medical device (K914059) manufactured by Nk Biotechnical Engineering Co.. 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 8, 1991. Regulation: 8.