CENTRE-DRIVE DRILL-FREE SCREW

CENTRE-DRIVE DRILL-FREE SCREW is an FDA 510(k)-cleared medical device (K971297) manufactured by KLS-Martin L.P.. 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 7, 1997. Regulation: 8.