510(k) K190779 ยท POL Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment
Trevo XP ProVue Retriever
| Applicant | Stryker, Fremont CA, US |
| Decision | Substantially Equivalent, Jun 25, 2019 |
| Received | Mar 27, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190779
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 21, 2020 | Stryker Neurovascular Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF: 80052, 93067, 93068, M0032PK42010001, M0033PK42022001, M0033PK43022001, M0033PK6 Terminated |
POL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.