
K2m, Inc.
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K2M, PYRENEES CERVICAL PLATE SYSTEM is an FDA 510(k)-cleared medical device (K113329) 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 January 16, 2012. Regulation: 8.