太平洋儀器骨科固定針及線材 / 克里斯琴器 / 引導線材
K 號：K213982 · 2022-02-17
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器材摘要
常見問題
What is the Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires?
Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires is a medical device that received FDA 510(k) clearance on 2022-02-17. The listed applicant is Pacific Instruments. The 510(k) number is K213982.
When did Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires receive FDA 510(k) clearance?
Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires received FDA 510(k) clearance on 2022-02-17, under 510(k) number K213982.
Who is the listed applicant for Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires?
The FDA 510(k) record lists Pacific Instruments as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires?
The FDA product code for Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires is HTY.
相關臨床試驗
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。
相關器械（代碼：HTY）
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。
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。
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