510(k) K022364 ยท HAW Neurological Stereotaxic Instrument
NAVITRACK SYSTEM TOTAL HIP REPLACEMENT,MODEL 900.200
| Applicant | Orthosoft, Inc., Montreal, CA |
| Decision | Substantially Equivalent, Feb 4, 2003 |
| Received | Jul 22, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022364
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.