FDA 510(k)

Trevo Trak 21 微导管

K 號：K261889 · 2026-07-01

決定日期2026-07-01

產品代碼QJP

諮詢委員會履歷

決定相當於

器材摘要

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.

常見問題

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.

其他以 Stryker Neurovascular 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K253032AXS Lift 颅内基底導管 K252694目標可拆式線圈 K251832InZone IST 分離系統；IZDS 連接線 K242289Excelsior XT-27 微导管，Excelsior XT-27 強化微导管，Excelsior XT-27 預成型微导管，Excelsior XT-27 強化預成型微导管 K243593AXS Lift 颅内基底導管 K241637回聲內顱底針心管

查看所有 25 項裝置 →

相關器械（代碼：QJP）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K260220路92醫療全長046進入系統Route 92 Medical, Inc.K26227770 神經導引針管Piraeus Medical, Inc.K261176Zoom 4S 管針Imperative Care, Inc.K254071p17 XR 微导管Wallaby Medical K260199SLIM 微导管Balt USA, LLC K253901蟻蟻88 接通導管Perfuze, Ltd.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。