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Osteomed Corp.
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2.0/2.4 CANNULATED SCREW SYSTEM is an FDA 510(k)-cleared medical device (K010783) manufactured by Osteomed 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 May 29, 2001. Regulation: 8.