← Back to catalogue
KeriFlex® MCP and PIP Finger Joint Prostheses
FDA 510(k)Class II (US FDA 510(k))
510(k) K211385
Identifiers
- 510(k) Number
- K211385 FDA 510(k)
- FDA Product Code
- KYJ FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.3230 FDA 510(k)
- Regulation Number
- 888.3230 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
KeriFlex® MCP and PIP Finger Joint Prostheses by Keri Medical SA — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K211385 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Keri Medical SA
Sources (1)
- FDA 510(k) K211385 24 fields · synced Jun 18, 2026