510(k) K040568 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
POLYETHER URETHANE MATERIAL CHANGE IN NEUROSTIMULATION LEADS
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 25, 2004 |
| Received | Mar 4, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K040568
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.