UTS 肽
K 號：K172251 · 2017-10-24
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器材摘要
UTS Stem is the device name listed in this FDA 510(k) record. The listed applicant is United Orthopedic Corporation. It received FDA 510(k) clearance on 2017-10-24 under 510(k) number K172251. 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 UTS Stem?
UTS Stem is a medical device that received FDA 510(k) clearance on 2017-10-24. The listed applicant is United Orthopedic Corporation. The 510(k) number is K172251.
When did UTS Stem receive FDA 510(k) clearance?
UTS Stem received FDA 510(k) clearance on 2017-10-24, under 510(k) number K172251.
Who is the listed applicant for UTS Stem?
FDA 510(k) 記錄中將 United Orthopedic Corporation 列為申請人。這並不單獨確立該設備製造商的身份。
What is the FDA product code for UTS Stem?
The FDA product code for UTS Stem is LPH.
其他以 United Orthopedic Corporation 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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