510(k) K032561 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
RESUME II LEAD KIT FOR SPINAL CORD STIMULATION (SCS) AND PERIPHERAL NERVE STIMULATION (PNS), RESUME TL LEAD KIT FOR
| Applicant | Medtronic Vascular, Miinneapolis MN, US |
| Decision | Substantially Equivalent, Sep 11, 2003 |
| Received | Aug 20, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032561
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.