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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 the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovascular. It received FDA 510(k) clearance on 2021-08-27 under 510(k) 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. The listed applicant is Stryker Neurovascular. The 510(k) number is K210502.

When did Trevo NXT ProVue Retriever receive FDA 510(k) clearance?

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

Who is the listed applicant for Trevo NXT ProVue Retriever?

The FDA 510(k) record lists Stryker Neurovascular as the applicant. This does not by itself establish the device manufacturer.

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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Other records listing Stryker Neurovascular as applicant

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Related Devices (Code: POL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242676pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy DevicePhenox LimitedK231539pRESET LITE Thrombectomy DevicePhenox LimitedK223305Trevo NXT ProVue RetrieverStryker NeurovascularK222848pRESET Thrombectomy DevicePhenox LimitedK203358Solitaire X Revascularization DeviceMicro Therapeutics, Inc. d/b/a ev3 NeurovascularK203219Trevo XP ProVue Retriever and Trevo NXT™ ProVue RetrieverStryker Neurovascular

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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