
Biomet Microfixation
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BIOMET MICROFIXATION NEURO PLATING SYSTEM is an FDA 510(k)-cleared medical device (K121624) manufactured by Biomet Microfixation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 11, 2012. Regulation: 8.