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AFFIXUS®JIG KNOB LARGE

Biomet Orthopedics, LLC · Model 211201212 · UDI-DI 00880304535985

HWD Prescription
0
510(k) clearances
28
Adverse events
1
Recalls
91
Facilities

Recalls

DateFirmReason
2011-03-10Biomet, Inc.One lot of 30 mm screws was switched with one lot of 25 mm screws.

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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.