510(k) K081713 ยท MOQ Battery, Replacement, Rechargeable
VERTEBRAL ACCESS SYSTEM BY VIDACARE
| Applicant | Vidacare Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Nov 21, 2008 |
| Received | Jun 17, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081713
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.