510(k) K163209 ยท HAW Neurological Stereotaxic Instrument
Fiagon Navigation System
| Applicant | Fiagon GmbH, Hennigsdorf, DE |
| Decision | Substantially Equivalent, Sep 14, 2017 |
| Received | Nov 15, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163209
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.