GROSSE AND KEMPF LOCKING NAIL SYS.

GROSSE AND KEMPF LOCKING NAIL SYS. is an FDA 510(k)-cleared medical device (K813371) manufactured by Howmedica Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 1982. Regulation: 8.