510(k) K955291 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
DUALSCREEN
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 17, 1996 |
| Received | Nov 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955291
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.