510(k) K100836 ยท ORR Neurological Stereotaxic Instrument, Real-Time Intraoperative Mri
CLEARPOINT SYSTEM
| Applicant | Surgivision, Inc., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Jun 16, 2010 |
| Received | Mar 24, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100836
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.