BARNES FEMORAL LENGTHENING DEVICE

BARNES FEMORAL LENGTHENING DEVICE is an FDA 510(k)-cleared medical device (K895243) manufactured by Piedmont Sports Medicine & Orthopaedic Clinic. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 9, 1990. Regulation: 8.