Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)— 510(k) K173352
Substantially EquivalentConcentric Medical, Inc.
FDA 510(k) clearance K173352 for Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever), Substantially Equivalent on 2018-02-15. Applicant: Concentric Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Concentric Medical, Inc.
- Product code
- Code POL
- Device class
- Class 2
- Regulation
- 21 CFR 882.5600
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mountain View, CA, US
Recent devices under product code POL
view allMore clearances from Concentric Medical, Inc.
view all- DEN150049 — Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mm
- K150616 — Trevo XP ProVue Retriever (4x30mm)
- K143077 — Trevo XP ProVue Retriever (6X25mm)
- K133177 — MODIFIED HD GUIDE CATHETER
- K133464 — MODIFIED TREVO PROVUE RETRIEVER
Recalls naming K173352
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K173352.
Data sourced from openFDA. This site is unofficial and independent of the FDA.