510(k) K130874 ยท HAW Neurological Stereotaxic Instrument
STRYKER NAV3I PLATFORM
| Applicant | Stryker Corporate, Freiburg, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, Sep 27, 2013 |
| Received | Mar 29, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130874
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.