DePuy 3D增材製造三邊緣骨盂杯
K 號：K201348 · 2022-06-16
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器材摘要
DePuy 3D Additive TriFlange Acetabular Cup is the device name listed in this FDA 510(k) record. The listed applicant is Depuy International, Ltd.. It received FDA 510(k) clearance on 2022-06-16 under 510(k) number K201348. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the DePuy 3D Additive TriFlange Acetabular Cup?
DePuy 3D Additive TriFlange Acetabular Cup is a medical device that received FDA 510(k) clearance on 2022-06-16. The listed applicant is Depuy International, Ltd.. The 510(k) number is K201348.
When did DePuy 3D Additive TriFlange Acetabular Cup receive FDA 510(k) clearance?
DePuy 3D Additive TriFlange Acetabular Cup received FDA 510(k) clearance on 2022-06-16, under 510(k) number K201348.
Who is the listed applicant for DePuy 3D Additive TriFlange Acetabular Cup?
The FDA 510(k) record lists Depuy International, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DePuy 3D Additive TriFlange Acetabular Cup?
The FDA product code for DePuy 3D Additive TriFlange Acetabular Cup is LPH.
相關臨床試驗
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相關器械（代碼：LPH）
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
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