510(k) K161879 ยท NRY Catheter, Thrombus Retriever
Solitaire Platinum Revascularization Device
| Applicant | Micro Therapeutics, Inc. d/b/a ev3 Neurovascular, Irvine CA, US |
| Decision | Substantially Equivalent, Sep 21, 2016 |
| Received | Jul 8, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161879
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.