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Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant

FDA product code PNW · Class 3 · Unknown

4
Registered devices
555
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Cartiva Synthetic Cartilage Implant — CARTIVA, INCCartiva Synthetic Cartilage Implant — CARTIVA, INCCartiva Synthetic Cartilage Implant — CARTIVA, INCCartiva Synthetic Cartilage Implant — CARTIVA, INC

Recent recalls

DateFirmReason
2024-10-31Cartiva, IncPatients implanted with synthetic cartilage implant, may experience a higher-than expected occurrence rate of the following hazards: revision, removal, implant

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.