510(k) K021327 ยท HAW Neurological Stereotaxic Instrument
ORTHOPILOT HTO MODULE
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jul 25, 2002 |
| Received | Apr 26, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021327
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.