510(k) K020631 ยท HAW Neurological Stereotaxic Instrument
IPLAN
| Applicant | Brainlab AG, Heimstetten, DE |
| Decision | Substantially Equivalent, Sep 9, 2002 |
| Received | Feb 27, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020631
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.