西爾克士大腿骨柄
K 號：K231109 · 2023-06-15
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器材摘要
Xerxes Hip Stem is the device name listed in this FDA 510(k) record. The listed applicant is Xerxes Arthopedix, LLC. It received FDA 510(k) clearance on 2023-06-15 under 510(k) number K231109. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Xerxes Hip Stem?
Xerxes Hip Stem is a medical device that received FDA 510(k) clearance on 2023-06-15. The listed applicant is Xerxes Arthopedix, LLC. The 510(k) number is K231109.
When did Xerxes Hip Stem receive FDA 510(k) clearance?
Xerxes Hip Stem received FDA 510(k) clearance on 2023-06-15, under 510(k) number K231109.
Who is the listed applicant for Xerxes Hip Stem?
The FDA 510(k) record lists Xerxes Arthopedix, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Xerxes Hip Stem?
The FDA product code for Xerxes Hip Stem is LZO.
相關臨床試驗
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相關器械（代碼：LZO）
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。
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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