Company ยท US
Relievant Medsystems
FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2022. Name variants (Inc, Corp, punctuation) are merged.
10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 26, 2022 | K222281 | Intracept Intraosseous Nerve Ablation System Relievant Medsystems, Inc. | GXI |
| Mar 11, 2022 | K213836 | Intracept Intraosseous Nerve Ablation System Relievant Medsystems, Inc. | GXI |
| May 3, 2019 | K190504 | Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instrument Relievant Medsystems | GXI |
| Sep 14, 2018 | K180369 | Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe) Relievant Medsystems | GXI |
| Aug 18, 2017 | K171143 | Relievant Medsystems RF Generator Relievant Medsystems | GXD |
| Aug 9, 2017 | K170827 | INTRACEPT Intraosseous Nerve Ablation System Relievant Medsystems | GXI |
| Jul 9, 2016 | K153272 | INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set Relievant Medsystems | GXI |
| Mar 30, 2010 | K100641 | INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND EASY ACCESS INSTRUMENT SET, MODEL FG0018 (PROBE), FG0036 (INSTRUMENT SET) Relievant Medsystems | GEI |
| Jan 22, 2009 | K083856 | INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026 Relievant Medsystems, Inc. | GEI |
| Oct 5, 2007 | K070443 | INTRACEPT BI-POLAR RF PROBE, MODEL 04814 Relievant Medsystems, Inc. | GEI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||