510(k) K101627 ยท HAW Neurological Stereotaxic Instrument
IPLAN
| Applicant | Brainlab AG, Feldkirchen, DE |
| Decision | Substantially Equivalent, Jun 3, 2011 |
| Received | Jun 9, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101627
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.