510(k) K920567 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
MODELS 3987 AND 3988 RESUME LEAD FOR PNS
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 20, 1992 |
| Received | Feb 7, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920567
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.