510(k) K002732 ยท HAW Neurological Stereotaxic Instrument
STRYKER NAVIGATION SYSTEM - ENT MODULE
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Oct 2, 2000 |
| Received | Sep 1, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002732
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.