510(k) K160434 ยท HAW Neurological Stereotaxic Instrument
ClearPoint System
| Applicant | Mri Interventions, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Mar 17, 2016 |
| Received | Feb 16, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160434
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.