510(k) K230780 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
MFG-05
| Applicant | Zimmer Medizinsysteme GmbH, Neu-Elm, DE |
| Decision | Substantially Equivalent, Oct 5, 2023 |
| Received | Mar 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230780
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.