MODUS SYSTEM SELF-DRILLING SCREWS

MODUS SYSTEM SELF-DRILLING SCREWS is an FDA 510(k)-cleared medical device (K992106) manufactured by Medartis 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 September 16, 1999. Regulation: 8.