解剖肩部系統,解剖肩部DomeLock系統,解剖肩部骨折系統
K 號:K160085 · 2016-03-08
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器材摘要
常見問題
What is the Anatomical Shoulder System, Anatomical Shoulder Domelock System, Anatomical Shoulder Fracture System?
Anatomical Shoulder System, Anatomical Shoulder Domelock System, Anatomical Shoulder Fracture System is a medical device that received FDA 510(k) clearance on 2016-03-08. The listed applicant is Zimmer GmbH. The 510(k) number is K160085.
When did Anatomical Shoulder System, Anatomical Shoulder Domelock System, Anatomical Shoulder Fracture System receive FDA 510(k) clearance?
Anatomical Shoulder System, Anatomical Shoulder Domelock System, Anatomical Shoulder Fracture System received FDA 510(k) clearance on 2016-03-08, under 510(k) number K160085.
Who is the listed applicant for Anatomical Shoulder System, Anatomical Shoulder Domelock System, Anatomical Shoulder Fracture System?
The FDA 510(k) record lists Zimmer GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Anatomical Shoulder System, Anatomical Shoulder Domelock System, Anatomical Shoulder Fracture System?
The FDA product code for Anatomical Shoulder System, Anatomical Shoulder Domelock System, Anatomical Shoulder Fracture System is KWS.
相關臨床試驗
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其他以 Zimmer GmbH 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。
相關器械(代碼:KWS)
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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