
Osteomed LP
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OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM is an FDA 510(k)-cleared medical device (K062863) manufactured by Osteomed LP. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 30, 2006. Regulation: 8.