Relievant Medsystems, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222281 | Intracept Intraosseous Nerve Ablation System | GXI | 2022-10-26 | View |
| 510(k) | K213836 | Intracept Intraosseous Nerve Ablation System | GXI | 2022-03-11 | View |
| 510(k) | K083856 | INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026 | GEI | 2009-01-22 | View |
| 510(k) | K070443 | INTRACEPT BI-POLAR RF PROBE, MODEL 04814 | GEI | 2007-10-05 | View |
No matching devices.
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