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Ascension Silicone MCP +1 more model
FDA 510(k)Class II (US FDA 510(k))
510(k) K233670
Identifiers
- 510(k) Number
- K233670 FDA 510(k)
- FDA Product Code
- KYJ FDA 510(k)
- Models / Variants
- Ascension Silicone MCP FDA 510(k)Ascension Silicone PIP 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)
Ascension Silicone MCP +1 more model by Ascension Orthopedics, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 2 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 | K233670 | Class II | Active |
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Manufacturer
- Manufacturer
- Ascension Orthopedics, Inc.
Sources (1)
- FDA 510(k) K233670 24 fields · synced Jun 19, 2026