AltiVate® Anatomic Shoulder AG e+™ with Markers
K 號:K213387 · 2022-07-07
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器材摘要
常見問題
What is the AltiVate® Anatomic Shoulder AG e+™ with Markers?
AltiVate® Anatomic Shoulder AG e+™ with Markers is a medical device that received FDA 510(k) clearance on 2022-07-07. The listed applicant is Encore Medical L.P.. The 510(k) number is K213387.
When did AltiVate® Anatomic Shoulder AG e+™ with Markers receive FDA 510(k) clearance?
AltiVate® Anatomic Shoulder AG e+™ with Markers received FDA 510(k) clearance on 2022-07-07, under 510(k) number K213387.
Who is the listed applicant for AltiVate® Anatomic Shoulder AG e+™ with Markers?
The FDA 510(k) record lists Encore Medical L.P. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AltiVate® Anatomic Shoulder AG e+™ with Markers?
The FDA product code for AltiVate® Anatomic Shoulder AG e+™ with Markers is KWS.
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。
其他以 Encore Medical L.P. 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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