510(k) K800193 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MEDTRONIC PISCES GENERATION II LEAD KIT
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Feb 5, 1980 |
| Received | Jan 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800193
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.