510(k) K952459 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MEDTRONIC MODEL 3991, 3991C, 3992, 3992C, 3993, 3993C, 3994, 3994C LEADS OR, TRANSVERSE TRIPOLAR LEADS OR, TTL
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 30, 1995 |
| Received | May 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952459
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.