骨質-P 骨移植代用品
K 號：K170165 · 2017-12-29
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器材摘要
Osteo-P Bone Graft Substitute is the device name listed in this FDA 510(k) record. The listed applicant is Molecular Matrix, Inc.. It received FDA 510(k) clearance on 2017-12-29 under 510(k) number K170165. 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 Osteo-P Bone Graft Substitute?
Osteo-P Bone Graft Substitute is a medical device that received FDA 510(k) clearance on 2017-12-29. The listed applicant is Molecular Matrix, Inc.. The 510(k) number is K170165.
When did Osteo-P Bone Graft Substitute receive FDA 510(k) clearance?
Osteo-P Bone Graft Substitute received FDA 510(k) clearance on 2017-12-29, under 510(k) number K170165.
Who is the listed applicant for Osteo-P Bone Graft Substitute?
The FDA 510(k) record lists Molecular Matrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Osteo-P Bone Graft Substitute?
The FDA product code for Osteo-P Bone Graft Substitute 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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