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Stryker MP, Mandible, HMMF and MMF AXS Screws
FDA 510(k)Class II (US FDA 510(k))
510(k) K231599
Identifiers
- 510(k) Number
- K231599 FDA 510(k)
- FDA Product Code
- DZL FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 872.4880 FDA 510(k)
- Regulation Number
- 872.4880 FDA 510(k)
- Advisory Committee
- Dental FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Stryker MP, Mandible, HMMF and MMF AXS Screws by Stryker Leibinger Gmbh & Co. Kg — 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 | K231599 | 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) K231599 24 fields · synced Jun 19, 2026