510(k) K832916 ยท LLE Stimulator, Spinal-Cord, Implanted For Peripheral Vascular Disease
INIVOX ELECTRODE/CATHETER SYS
| Applicant | Critikon Company, LLC, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 14, 1983 |
| Received | Aug 29, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832916
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.