Identifiers
- 510(k) Number
- K061451 FDA 510(k)
- FDA Product Code
- KYI FDA 510(k)
- Models / Variants
- Cmc-400 FDA 510(k)13 FDA 510(k)Cmc-400-20 FDA 510(k)Cmc-400-30 FDA 510(k)Cmc-400-40 FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.3770 FDA 510(k)
- Regulation Number
- 888.3770 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Ascension (Cmc-400 +4 more) by Ascension Orthopedics, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 5 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 | K061451 | Class II | Active |
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Manufacturer
- Manufacturer
- Ascension Orthopedics, Inc.
Sources (1)
- FDA 510(k) K061451 24 fields · synced Jun 19, 2026