510(k) K062201 ยท NFA Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection
SPIDERX EMBOLIC PROTECTION DEVICE
| Applicant | Ev3, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Aug 11, 2006 |
| Received | Aug 1, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062201
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.