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Toe Mp Joint (10412-10414 +6 more)
FDA 510(k)Class II (US FDA 510(k))
510(k) K041595
by Biopro, Inc.
Identifiers
- 510(k) Number
- K041595 FDA 510(k)
- FDA Product Code
- KWD FDA 510(k)
- Models / Variants
- 10412-10414 FDA 510(k)14958 FDA 510(k)14960 FDA 510(k)1060-10062 FDA 510(k)16818 FDA 510(k)-16822 FDA 510(k)16867-16870 FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.3730 FDA 510(k)
- Regulation Number
- 888.3730 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Toe Mp Joint (10412-10414 +6 more) by Biopro, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 7 models — 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 | K041595 | Class II | Active |
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Manufacturer
- Manufacturer
- Biopro, Inc.
Sources (1)
- FDA 510(k) K041595 24 fields · synced Jun 18, 2026