510(k) K022222 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
LAMITRODE S-SERIES (S4 AND S8) LEADS
| Applicant | Advanced Neuromodulation System,Inc, Plano TX, US |
| Decision | Substantially Equivalent, Aug 8, 2002 |
| Received | Jul 9, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022222
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.