510(k) K123390 ยท PDQ Neurosurgical Nerve Locator
PEDIGUARD NERVE DETECTOR SYSTEM
| Applicant | Spineguard S.A., Washington DC, US |
| Decision | Substantially Equivalent, Aug 8, 2013 |
| Received | Nov 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123390
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.