Simparo 鍵盤線固定系統
K 號：K222574 · 2023-02-04
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器材摘要
Simparo Anchor Line Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Simparo, Inc.. It received FDA 510(k) clearance on 2023-02-04 under 510(k) number K222574. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Simparo Anchor Line Fixation System?
Simparo Anchor Line Fixation System is a medical device that received FDA 510(k) clearance on 2023-02-04. The listed applicant is Simparo, Inc.. The 510(k) number is K222574.
When did Simparo Anchor Line Fixation System receive FDA 510(k) clearance?
Simparo Anchor Line Fixation System received FDA 510(k) clearance on 2023-02-04, under 510(k) number K222574.
Who is the listed applicant for Simparo Anchor Line Fixation System?
The FDA 510(k) record lists Simparo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Simparo Anchor Line Fixation System?
The FDA product code for Simparo Anchor Line Fixation System is MBI.
相關臨床試驗
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相關器械（代碼：MBI）
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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