OSTEO INTERLOCKING-COMPRESSION NAIL

OSTEO INTERLOCKING-COMPRESSION NAIL is an FDA 510(k)-cleared medical device (K933340) manufactured by Osteo AG. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 29, 1994. Regulation: 8.