510(k) K014256 ยท HAW Neurological Stereotaxic Instrument
KOLIBRI IGS SYSTEMS
| Applicant | Brainlab AG, Heimstetten, DE |
| Decision | Substantially Equivalent, Jul 19, 2002 |
| Received | Dec 26, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014256
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.