KRONNER UNIVERSAL FRAME EXTERNAL FIXATION

KRONNER UNIVERSAL FRAME EXTERNAL FIXATION is an FDA 510(k)-cleared medical device (K871247) manufactured by Kronner Medical. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 1987. Regulation: 8.