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Stryker CMF MEDPOR Priority Customized Implant Kit
FDA 510(k)Class II (US FDA 510(k))
510(k) K191916
Identifiers
- 510(k) Number
- K191916 FDA 510(k)
- FDA Product Code
- FWP FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.3550 FDA 510(k)
- Regulation Number
- 878.3550 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Stryker CMF MEDPOR Priority Customized Implant Kit by Stryker Leibinger Gmbh & Co. Kg — Class II — FDA_510K — listed in FDA 510(k)
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 | K191916 | Class II | Active |
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Manufacturer
- Manufacturer
- Stryker Leibinger Gmbh & Co. Kg
- FDA Applicant
- Stryker Leibinger GmbH & Co KG
Sources (1)
- FDA 510(k) K191916 24 fields · synced Jun 18, 2026