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1.5MM SYSTEM

BIOMET MICROFIXATION, INC · Model 01-7249 · UDI-DI 00841036134792

GXRHBWJEYGWO Prescription
3
510(k) clearances
210
Adverse events
1
Recalls
52
Facilities

Recalls

DateFirmReason
2021-06-02Medtronic NeuromodulationExcess nylon flash on the clip.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.