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DISTRACTION SYSTEM

BIOMET MICROFIXATION, INC · Model 01-3556 · UDI-DI 00841036010867

HXX Prescription
4
510(k) clearances
23,582
Adverse events (4 deaths)
0
Recalls
465
Facilities

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.