510(k) K964172 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MEDTRONIC MODEL 3991A, 3992A, 3993A, 3994A LEADS OR TRANSVERSE TRIPOLAR LEADS OR TTL
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 3, 1997 |
| Received | Oct 18, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964172
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.