Taperloc® 完整股骨柄
K 號：K251270 · 2026-05-19
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器材摘要
Taperloc® Complete Hip Stem is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2026-05-19 under 510(k) number K251270. 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 Taperloc® Complete Hip Stem?
Taperloc® Complete Hip Stem is a medical device that received FDA 510(k) clearance on 2026-05-19. The listed applicant is Biomet, Inc.. The 510(k) number is K251270.
When did Taperloc® Complete Hip Stem receive FDA 510(k) clearance?
Taperloc® Complete Hip Stem received FDA 510(k) clearance on 2026-05-19, under 510(k) number K251270.
Who is the listed applicant for Taperloc® Complete Hip Stem?
The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Taperloc® Complete Hip Stem?
The FDA product code for Taperloc® Complete Hip Stem is LPH.
相關臨床試驗
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其他以 Biomet, Inc. 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：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
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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