510(k) K033011 ยท HAW Neurological Stereotaxic Instrument
ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 12, 2004 |
| Received | Sep 26, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033011
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.