AltiVate Reverse Humeral Stem, 48mm
K 號：K190290 · 2019-04-26
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器材摘要
AltiVate Reverse Humeral Stem, 48mm is the device name listed in this FDA 510(k) record. The listed applicant is Encore Medical L.P.. It received FDA 510(k) clearance on 2019-04-26 under 510(k) number K190290. The device is classified under product code KWS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the AltiVate Reverse Humeral Stem, 48mm?
AltiVate Reverse Humeral Stem, 48mm is a medical device that received FDA 510(k) clearance on 2019-04-26. The listed applicant is Encore Medical L.P.. The 510(k) number is K190290.
When did AltiVate Reverse Humeral Stem, 48mm receive FDA 510(k) clearance?
AltiVate Reverse Humeral Stem, 48mm received FDA 510(k) clearance on 2019-04-26, under 510(k) number K190290.
Who is the listed applicant for AltiVate Reverse Humeral Stem, 48mm?
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 Reverse Humeral Stem, 48mm?
The FDA product code for AltiVate Reverse Humeral Stem, 48mm is KWS.
相關臨床試驗
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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。
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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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