510(k) K160593 ยท MMX Device, Percutaneous Retrieval
Indy OTW Vascular Retriever
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, Sep 2, 2016 |
| Received | Mar 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160593
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.