510(k) K991706 ยท HAW Neurological Stereotaxic Instrument
VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Dec 7, 1999 |
| Received | May 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991706
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.