FDA 510(k)

礦物膠原蛋白複合生物活性可塑骨移植基质

K 號：K240424 · 2024-03-12

決定日期2024-03-12

產品代碼MQV

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決定相當於

器材摘要

Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2024-03-12 under 510(k) number K240424. 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 Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix?

Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix is a medical device that received FDA 510(k) clearance on 2024-03-12. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K240424.

When did Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix receive FDA 510(k) clearance?

Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix received FDA 510(k) clearance on 2024-03-12, under 510(k) number K240424.

Who is the listed applicant for Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix?

The FDA 510(k) record lists Collagen Matrix, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix?

The FDA product code for Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix is MQV.

其他以 Collagen Matrix, Inc. 為申請人之記錄

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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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