510(k) K213813 ยท FZP Clip, Implantable
DuraFuse Clip and Applier System
| Applicant | Neuramedica, Inc., Oregon City OR, US |
| Decision | Substantially Equivalent, Jul 22, 2022 |
| Received | Dec 7, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213813
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.