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FDA 510(k)

Trevo XP ProVue Retriever

K-Number: K190779 · 2019-06-25

ApplicantStryker
Decision Date2019-06-25
Product CodePOL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Trevo XP ProVue Retriever is a medical device manufactured by Stryker. It received FDA 510(k) clearance on 2019-06-25 under approval number K190779. The device is classified under product code POL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trevo XP ProVue Retriever?

Trevo XP ProVue Retriever is a medical device that received FDA 510(k) clearance on 2019-06-25. It is manufactured by Stryker. The 510(k) number is K190779.

When was Trevo XP ProVue Retriever approved by the FDA?

Trevo XP ProVue Retriever received FDA 510(k) clearance on 2019-06-25, under approval number K190779.

What company makes Trevo XP ProVue Retriever?

Trevo XP ProVue Retriever is manufactured by Stryker.

What is the FDA product code for Trevo XP ProVue Retriever?

The FDA product code for Trevo XP ProVue Retriever is POL.

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Related Devices (Code: POL)

K162539Solitaire 2 Revascularization DeviceMicro Therapeutics, Inc. d/b/a ev3 Neurovascular DEN150049Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mmConcentric Medical, Inc. K181186Solitare Platinum Revascularization DeviceMicro Therapeutics, Inc. d/b/a ev3 Neurovascular K181060Solitaire 2 and Solitaire Platinum Revascularization DeviceMedtronic Neurovascular K173352Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)Concentric Medical, Inc. K192207Trevo NXT ProVue RetrieverStryker

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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