Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)
FDA 510(k) clearance K173352 · decided 2018-02-15
Clearance details
- K-number
- K173352
- Device name
- Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)
- Applicant
- Concentric Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2017-10-25
- Decision date
- 2018-02-15
- Days to decision
- 113 days
- Clearance type
- Traditional
- Product code
- POL
- Device class
- 2
- Regulation number
- 882.5600
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Mountain View, CA, US
- Third-party review
- No
- Expedited review
- Yes
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Trevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catalog recall (Z-1902-2024) | Stryker Neurovascular | 2024-05-28 |