
Biomet Microfixation, Inc.
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BIOMET MICROFIXATION LACTOSORB PECTUS STABILIZER is an FDA 510(k)-cleared medical device (K071577) manufactured by Biomet Microfixation, 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 September 5, 2007. Regulation: 8.