510(k) K052659 ยท NTE Temporary Carotid Catheter For Embolic Capture
SPIDERX EMBOLIC PROTECTION DEVICE
| Applicant | Ev3, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 17, 2006 |
| Received | Sep 27, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052659
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.