510(k) K021760 ยท HAW Neurological Stereotaxic Instrument
NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120
| Applicant | Orthosoft, Inc., Montreal, CA |
| Decision | Substantially Equivalent, Aug 27, 2002 |
| Received | May 29, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021760
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.