Refobacin骨水泥R (110034355)
K 號：K254107 · 2026-04-15
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器材摘要
Refobacin Bone Cement R (110034355) is the device name listed in this FDA 510(k) record. The listed applicant is Biomet France. It received FDA 510(k) clearance on 2026-04-15 under 510(k) number K254107. The device is classified under product code LOD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Refobacin Bone Cement R (110034355)?
Refobacin Bone Cement R (110034355) is a medical device that received FDA 510(k) clearance on 2026-04-15. The listed applicant is Biomet France. The 510(k) number is K254107.
When did Refobacin Bone Cement R (110034355) receive FDA 510(k) clearance?
Refobacin Bone Cement R (110034355) received FDA 510(k) clearance on 2026-04-15, under 510(k) number K254107.
Who is the listed applicant for Refobacin Bone Cement R (110034355)?
The FDA 510(k) record lists Biomet France as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Refobacin Bone Cement R (110034355)?
The FDA product code for Refobacin Bone Cement R (110034355) is LOD.
相關臨床試驗
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相關器械（代碼：LOD）
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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