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FDA 510(k)

Trevo NXT ProVue Retriever

K-Number: K210502 · 2021-08-27

ApplicantStryker Neurovascular
Decision Date2021-08-27
Product CodePOL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Trevo NXT ProVue Retriever is a medical device manufactured by Stryker Neurovascular. It received FDA 510(k) clearance on 2021-08-27 under approval number K210502. 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 NXT ProVue Retriever?

Trevo NXT ProVue Retriever is a medical device that received FDA 510(k) clearance on 2021-08-27. It is manufactured by Stryker Neurovascular. The 510(k) number is K210502.

When was Trevo NXT ProVue Retriever approved by the FDA?

Trevo NXT ProVue Retriever received FDA 510(k) clearance on 2021-08-27, under approval number K210502.

What company makes Trevo NXT ProVue Retriever?

Trevo NXT ProVue Retriever is manufactured by Stryker Neurovascular.

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

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

Related Clinical Trials

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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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