
Doctor'S Research Group, Inc.
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DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM is an FDA 510(k)-cleared medical device (K974817) manufactured by Doctor'S Research Group, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 1998. Regulation: 8.