510(k) K013569 ยท HAW Neurological Stereotaxic Instrument
ORTHOPILOT 2
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Apr 4, 2002 |
| Received | Oct 29, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013569
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.