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FDA 510(k)

統一U2股骨頭,22mm三角陶瓷頭

K 號:K221675 · 2022-11-04

決定日期2022-11-04
產品代碼LPH
諮詢委員會或
決定相當於

器材摘要

United U2 femoral head, 22mm delta ceramic head 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 2022-11-04 under 510(k) number K221675. 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 United U2 femoral head, 22mm delta ceramic head?

United U2 femoral head, 22mm delta ceramic head is a medical device that received FDA 510(k) clearance on 2022-11-04. The listed applicant is United Orthopedic Corporation. The 510(k) number is K221675.

When did United U2 femoral head, 22mm delta ceramic head receive FDA 510(k) clearance?

United U2 femoral head, 22mm delta ceramic head received FDA 510(k) clearance on 2022-11-04, under 510(k) number K221675.

Who is the listed applicant for United U2 femoral head, 22mm delta ceramic head?

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 United U2 femoral head, 22mm delta ceramic head?

The FDA product code for United U2 femoral head, 22mm delta ceramic head is LPH.

相關臨床試驗

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其他以 United Orthopedic Corporation 為申請人之記錄

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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。

官方來源

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