FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)

K Number: K173352 · Decision Feb 15, 2018
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
17
Applicant Total
45
Review Days
113

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Basic Information

Device Name
Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)
K Number
K173352
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5600
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Concentric Medical, Inc.
Date Received
October 25, 2017
Decision Date
February 15, 2018
Product Code
POL
Advisory Committee
Neurology
Review Advisory Committee
NE
Expedited Review
Y
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
POL Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (POL), ordered by most recent decision date.

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Other Clearances by Concentric Medical, Inc.

K Number Device Name
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
K132641 MODIFIED TREVO PROVUE RETRIEVER
K131437 MODIFIED CONCENTRIC MICROCATHETER
K131492 MODIFIED FLOWGATE BALLOON GUIDE CATHETER
K122581 MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254
K122478 MODIFIED TREVO RETRIEVER
Search all 45 clearances from Concentric Medical, Inc. →