MatrixRIB Fixation System
K 號：K161590 · 2016-11-03
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器材摘要
MatrixRIB Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (USA) Products, LLC. It received FDA 510(k) clearance on 2016-11-03 under 510(k) number K161590. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MatrixRIB Fixation System?
MatrixRIB Fixation System is a medical device that received FDA 510(k) clearance on 2016-11-03. The listed applicant is Synthes (USA) Products, LLC. The 510(k) number is K161590.
When did MatrixRIB Fixation System receive FDA 510(k) clearance?
MatrixRIB Fixation System received FDA 510(k) clearance on 2016-11-03, under 510(k) number K161590.
Who is the listed applicant for MatrixRIB Fixation System?
The FDA 510(k) record lists Synthes (USA) Products, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MatrixRIB Fixation System?
The FDA product code for MatrixRIB Fixation System is HRS.
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其他以 Synthes (USA) Products, LLC 為申請人之記錄
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相關器械（代碼：HRS）
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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