ExoToe 鋼釘
K 號：K172205 · 2018-01-11
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器材摘要
ExoToe Staple is the device name listed in this FDA 510(k) record. The listed applicant is Exotoe, LLC. It received FDA 510(k) clearance on 2018-01-11 under 510(k) number K172205. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ExoToe Staple?
ExoToe Staple is a medical device that received FDA 510(k) clearance on 2018-01-11. The listed applicant is Exotoe, LLC. The 510(k) number is K172205.
When did ExoToe Staple receive FDA 510(k) clearance?
ExoToe Staple received FDA 510(k) clearance on 2018-01-11, under 510(k) number K172205.
Who is the listed applicant for ExoToe Staple?
The FDA 510(k) record lists Exotoe, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ExoToe Staple?
The FDA product code for ExoToe Staple is JDR.
相關臨床試驗
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相關器械（代碼：JDR）
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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