510(k) K142432 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
StimRouter Lead Kit/StimRouter Surgical Tool Kit/StimRouter Clinician Kit/StimRouter User Kit
| Applicant | Bioness, Inc., Valencia CA, US |
| Decision | Substantially Equivalent, Feb 20, 2015 |
| Received | Aug 29, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142432
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.