510(k) K170827 ยท GXI Probe, Radiofrequency Lesion
INTRACEPT Intraosseous Nerve Ablation System
| Applicant | Relievant Medsystems, Redwood City CA, US |
| Decision | Substantially Equivalent, Aug 9, 2017 |
| Received | Mar 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170827
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.