510(k) K010204 ยท HAW Neurological Stereotaxic Instrument
STRYKER NAVIGATION SYSTEM-KNEE MODULE
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Aug 31, 2001 |
| Received | Jan 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010204
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.