510(k) K123378 ยท NRY Catheter, Thrombus Retriever
SOLITAIRE 2 REVASCULARIZATION DEVICE
| Applicant | Micro Therapeutics Dba Ev3 Neurovascular, Irvine CA, US |
| Decision | Substantially Equivalent, Nov 30, 2012 |
| Received | Nov 1, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123378
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.