510(k) K960631 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
MEDTRONIC MODEL 3550 ACCESSORY KIT (CONTENTS) 3550-OX
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 21, 1996 |
| Received | Feb 14, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960631
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.