
K2m, Inc.
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CAYMAN SCREWS MODEL K2-12-1000-XX, K2-12-1001-XX is an FDA 510(k)-cleared medical device (K100061) manufactured by K2m, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 11, 2010. Regulation: 8.