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Exactech, Inc. · Model 113-03-02 · UDI-DI 10885862016867

HWM Prescription
3
510(k) clearances
767
Adverse events
0
Recalls
254
Facilities

Description

OSTEOTOME, BOX

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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.