510(k) K082060 ยท HAW Neurological Stereotaxic Instrument
CRANIAL IMAGE GUIDED SURGERY SYSTEM
| Applicant | Brainlab AG, Feldkirchen, DE |
| Decision | Substantially Equivalent, May 8, 2009 |
| Received | Jul 21, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082060
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.