510(k) K120402 ยท DTK Filter, Intravascular, Cardiovascular
CRUX VENA CAVA FILTER SYSTEM
| Applicant | Crux Biomedical, Menlo Park CA, US |
| Decision | Substantially Equivalent, Jul 13, 2012 |
| Received | Feb 8, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120402
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.