三叉極端固定系統
K 號：K171690 · 2018-05-08
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器材摘要
Trident Extremity Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Trident Orthopedics. It received FDA 510(k) clearance on 2018-05-08 under 510(k) number K171690. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Trident Extremity Fixation System?
Trident Extremity Fixation System is a medical device that received FDA 510(k) clearance on 2018-05-08. The listed applicant is Trident Orthopedics. The 510(k) number is K171690.
When did Trident Extremity Fixation System receive FDA 510(k) clearance?
Trident Extremity Fixation System received FDA 510(k) clearance on 2018-05-08, under 510(k) number K171690.
Who is the listed applicant for Trident Extremity Fixation System?
The FDA 510(k) record lists Trident Orthopedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trident Extremity Fixation System?
The FDA product code for Trident Extremity Fixation System is HRS.
相關臨床試驗
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相關器械（代碼：HRS）
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。
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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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