extremity 全針織系統
K 號：K241695 · 2024-09-12
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器材摘要
Extremity All Suture System is the device name listed in this FDA 510(k) record. The listed applicant is Field Orthopaedics. It received FDA 510(k) clearance on 2024-09-12 under 510(k) number K241695. 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 Extremity All Suture System?
Extremity All Suture System is a medical device that received FDA 510(k) clearance on 2024-09-12. The listed applicant is Field Orthopaedics. The 510(k) number is K241695.
When did Extremity All Suture System receive FDA 510(k) clearance?
Extremity All Suture System received FDA 510(k) clearance on 2024-09-12, under 510(k) number K241695.
Who is the listed applicant for Extremity All Suture System?
The FDA 510(k) record lists Field Orthopaedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Extremity All Suture System?
The FDA product code for Extremity All Suture 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
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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