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FuzeFix Max FT
FUSION ORTHOPEDICS, LLC · Model CD-CS-0950 · UDI-DI 00840124521674
LRN
Prescription
1
510(k) clearances
1,208
Adverse events (2 deaths)
1
Recalls
40
Facilities
Description
Chamfered Screw Jig Set Wire
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-09-10 | Exactech, Inc. | Potential for the wire to fracture at the threads and remain in the glenoid. |
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Get your free API keyRead the docsData 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.