510(k) K912764 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MEDTRONIC MODEL 3861 TEMPORARY SCREENING LEAD KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 22, 1991 |
| Received | Jun 24, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912764
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.