帕尼頓近端股骨重建（PFR）系統
K 號：K241059 · 2025-01-13
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器材摘要
Pantheon Proximal Femur Reconstruction (PFR) System is the device name listed in this FDA 510(k) record. The listed applicant is Adler Ortho S.P.A. It received FDA 510(k) clearance on 2025-01-13 under 510(k) number K241059. 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 Pantheon Proximal Femur Reconstruction (PFR) System?
Pantheon Proximal Femur Reconstruction (PFR) System is a medical device that received FDA 510(k) clearance on 2025-01-13. The listed applicant is Adler Ortho S.P.A. The 510(k) number is K241059.
When did Pantheon Proximal Femur Reconstruction (PFR) System receive FDA 510(k) clearance?
Pantheon Proximal Femur Reconstruction (PFR) System received FDA 510(k) clearance on 2025-01-13, under 510(k) number K241059.
Who is the listed applicant for Pantheon Proximal Femur Reconstruction (PFR) System?
The FDA 510(k) record lists Adler Ortho S.P.A as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pantheon Proximal Femur Reconstruction (PFR) System?
The FDA product code for Pantheon Proximal Femur Reconstruction (PFR) System 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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