MCP骨膠
K 號：K160446 · 2016-11-07
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器材摘要
MCP Bone Putty is the device name listed in this FDA 510(k) record. The listed applicant is Biostructures, LLC. It received FDA 510(k) clearance on 2016-11-07 under 510(k) number K160446. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MCP Bone Putty?
MCP Bone Putty is a medical device that received FDA 510(k) clearance on 2016-11-07. The listed applicant is Biostructures, LLC. The 510(k) number is K160446.
When did MCP Bone Putty receive FDA 510(k) clearance?
MCP Bone Putty received FDA 510(k) clearance on 2016-11-07, under 510(k) number K160446.
Who is the listed applicant for MCP Bone Putty?
The FDA 510(k) record lists Biostructures, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MCP Bone Putty?
The FDA product code for MCP Bone Putty is MQV.
相關臨床試驗
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：MQV）
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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