510(k) K000852 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
RENEW NEUROSTIMULATION SYSTEM
| Applicant | Advanced Neuromodulation Systems, Plano TX, US |
| Decision | Substantially Equivalent, Jan 19, 2001 |
| Received | Mar 15, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000852
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.