510(k) K000105 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),
| Applicant | Medtronic Vascular, Minnetonka MN, US |
| Decision | Substantially Equivalent, Apr 12, 2000 |
| Received | Jan 14, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000105
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.