FDA 510(k)

Trevo Trak 21 Microcatheter

K-Number: K261889 · 2026-07-01

Decision Date2026-07-01

Product CodeQJP

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Trevo Trak 21 Microcatheter is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovascular. It received FDA 510(k) clearance on 2026-07-01 under 510(k) number K261889. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trevo Trak 21 Microcatheter?

Trevo Trak 21 Microcatheter is a medical device that received FDA 510(k) clearance on 2026-07-01. The listed applicant is Stryker Neurovascular. The 510(k) number is K261889.

When did Trevo Trak 21 Microcatheter receive FDA 510(k) clearance?

Trevo Trak 21 Microcatheter received FDA 510(k) clearance on 2026-07-01, under 510(k) number K261889.

Who is the listed applicant for Trevo Trak 21 Microcatheter?

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 Trak 21 Microcatheter?

The FDA product code for Trevo Trak 21 Microcatheter is QJP.

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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.