510(k) K013861 ยท HAW Neurological Stereotaxic Instrument
MODIFICATION TO LEKSELL SURGIPLAN WITH ATLASPACE
| Applicant | Elekta Instrument AB, Lake Forest CA, US |
| Decision | Substantially Equivalent, Dec 6, 2001 |
| Received | Nov 21, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013861
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.