510(k) K062358 ยท HAW Neurological Stereotaxic Instrument
MODIFICATION TO VECTORVISION TRAUMA
| Applicant | Brainlab AG, Feldkirchen, DE |
| Decision | Substantially Equivalent, Jan 17, 2007 |
| Received | Aug 14, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062358
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.