XenMatrix AB 外科移植物
K 號：K162193 · 2016-12-23
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器材摘要
XenMatrix AB Surgical Graft is the device name listed in this FDA 510(k) record. The listed applicant is C. R. Bard. It received FDA 510(k) clearance on 2016-12-23 under 510(k) number K162193. The device is classified under product code PIJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the XenMatrix AB Surgical Graft?
XenMatrix AB Surgical Graft is a medical device that received FDA 510(k) clearance on 2016-12-23. The listed applicant is C. R. Bard. The 510(k) number is K162193.
When did XenMatrix AB Surgical Graft receive FDA 510(k) clearance?
XenMatrix AB Surgical Graft received FDA 510(k) clearance on 2016-12-23, under 510(k) number K162193.
Who is the listed applicant for XenMatrix AB Surgical Graft?
The FDA 510(k) record lists C. R. Bard as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XenMatrix AB Surgical Graft?
The FDA product code for XenMatrix AB Surgical Graft is PIJ.
相關臨床試驗
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其他以 C. R. Bard 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。
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官方來源
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