依賴式頸椎IBF系統
K 號：K173102 · 2017-12-29
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器材摘要
Reliance Cervical IBF System is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Medical Systems, LLC. It received FDA 510(k) clearance on 2017-12-29 under 510(k) number K173102. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Reliance Cervical IBF System?
Reliance Cervical IBF System is a medical device that received FDA 510(k) clearance on 2017-12-29. The listed applicant is Reliance Medical Systems, LLC. The 510(k) number is K173102.
When did Reliance Cervical IBF System receive FDA 510(k) clearance?
Reliance Cervical IBF System received FDA 510(k) clearance on 2017-12-29, under 510(k) number K173102.
Who is the listed applicant for Reliance Cervical IBF System?
The FDA 510(k) record lists Reliance Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reliance Cervical IBF System?
The FDA product code for Reliance Cervical IBF System is ODP.
相關臨床試驗
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其他以 Reliance Medical Systems, LLC 為申請人之記錄
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。
相關器械（代碼：ODP）
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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