510(k) K780001 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
EPIDURAL LEAD - MODEL 3481
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Jan 17, 1978 |
| Received | Dec 30, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780001
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.