510(k) K162929 ยท HAW Neurological Stereotaxic Instrument
Stryker Navigation System with CranialMap software application, Stryker CranialMap Planning software application, Stryker CranialMask Tracker
| Applicant | Stryker Corporation, Freiburg Baden-Wurttemberg, DE |
| Decision | Substantially Equivalent, Feb 22, 2017 |
| Received | Oct 19, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162929
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.