Trevo NXT ProVue Retriever

Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment

Stryker Neurovascular

The following data is part of a premarket notification filed by Stryker Neurovascular with the FDA for Trevo Nxt Provue Retriever.

Pre-market Notification Details

Device IDK210502
510k NumberK210502
Device Name:Trevo NXT ProVue Retriever
ClassificationNeurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment
Applicant Stryker Neurovascular 47900 Bayside Parkway Fremont,  CA  94538
ContactRebecca Rosman
CorrespondentAshley Twitty
Stryker 47900 Bayside Parkway Fremont,  CA  94538
Product CodePOL  
CFR Regulation Number882.5600 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-02-22
Decision Date2021-08-27

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