510(k) K050752 ยท HAW Neurological Stereotaxic Instrument
AESCULAP ORTHOPILOT 2 THA V 2.0
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Apr 27, 2005 |
| Received | Mar 23, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050752
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.