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MISHA® Trial, Small, Right
Moximed, Inc. · Model 2-2002 · UDI-DI 00856047005863
QVV
Prescription
1
510(k) clearances
15
Adverse events
1
Recalls
3
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-02 | Moximed, Inc. | Knee implant may fracture due to a supplier-related issue with one component that has nonconforming geometry at the distal end of the absorber component that may result in a reduce |
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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.
