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Cartiva Synthetic Cartilage Implant
CARTIVA, INC · Model CAR-12-US · UDI-DI 00852897002335
PNW
Prescription
0
510(k) clearances
583
Adverse events
1
Recalls
2
Facilities
Description
12 mm Synthetic Cartilage Implant
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-10-31 | Cartiva, Inc | Patients implanted with synthetic cartilage implant, may experience a higher-than expected occurrence rate of the following hazards: revision, removal, implant subsidence, displace |
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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.