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Paradigm Interspinous Fusion Plate
FDA 510(k)Class II (US FDA 510(k))
510(k) K093438
Identifiers
- 510(k) Number
- K093438 FDA 510(k)
- FDA Product Code
- KWP FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.3050 FDA 510(k)
- Regulation Number
- 888.3050 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Paradigm Interspinous Fusion Plate by Paradigm Spine, LLC — 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 | K093438 | Class II | Active |
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Manufacturer
- Manufacturer
- Paradigm Spine, LLC
Sources (1)
- FDA 510(k) K093438 24 fields · synced Jun 18, 2026