510(k) K102523 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MULTI-LEAD TRIALING CABLE MODEL 355531
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 26, 2010 |
| Received | Sep 2, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102523
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.