510(k) K180981 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
Stimulator Kit, Trial Kit, Spare Lead Kit, Wearable Assembly Kit
| Applicant | Stimwave Technologies Incorporated, Pompano Beach FL, US |
| Decision | Substantially Equivalent, Sep 19, 2018 |
| Received | Apr 13, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180981
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.