510(k) K884948 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MODEL 3587A RESUME EPIDURAL LEAD
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 17, 1989 |
| Received | Nov 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884948
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.