510(k) K160523 ยท HAW Neurological Stereotaxic Instrument
BrightMatter Guide with BrightMatter Pointer
| Applicant | Synaptive Medical, Inc., Toronto, CA |
| Decision | Substantially Equivalent, Jun 24, 2016 |
| Received | Feb 25, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160523
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.