510(k) K012564 ยท HAW Neurological Stereotaxic Instrument
MODIFICATION TO: VECTORVISION FRAMELESS BIOPSY SYSTEM
| Applicant | Brainlab AG, Heimstetten, DE |
| Decision | Substantially Equivalent, Sep 6, 2001 |
| Received | Aug 9, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012564
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.