510(k) K173352 ยท POL Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment
Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)
| Applicant | Concentric Medical, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Feb 15, 2018 |
| Received | Oct 25, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173352
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 28, 2024 | Stryker Neurovascular Trevo XP ProVue Retriever 4 x 20, Catalog: 90182
Trevo XP ProVue Retriever 3 x 20, Catalog: 90183
Trevo XP ProVue Retriever 4 x 30, Catalog: 90185
Trevo XP ProVue Retriever 6 x 25, Catalog: 90186
Kit Open, Classified |
POL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.