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Spine Guidance 5.3 Software +3 more models
FDA 510(k)Class II (US FDA 510(k))
510(k) K252871
Identifiers
- 510(k) Number
- K252871 FDA 510(k)
- FDA Product Code
- OLO FDA 510(k)
- Models / Variants
- Spine Guidance 5.3 Software FDA 510(k)Q Interbody Instruments FDA 510(k)Elite Q Attachments FDA 510(k)Elite Cutting Accessories FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 882.4560 FDA 510(k)
- Regulation Number
- 882.4560 FDA 510(k)
- Advisory Committee
- Neurology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Spine Guidance 5.3 Software +3 more models by Stryker Leibinger Gmbh & Co. Kg — Class II — FDA_510K — listed in FDA 510(k) — 4 models
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 | K252871 | 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) K252871 24 fields · synced Jun 18, 2026