510(k) K062041 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MODEL 3875 1 X 8 SC TEST STIMULATION LEAD
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 16, 2006 |
| Received | Jul 19, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062041
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.