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FDA 510(k)

Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix

K-Number: K240424 · 2024-03-12

Decision Date2024-03-12
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix is a medical device manufactured by Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2024-03-12 under approval number K240424. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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. It is manufactured by Collagen Matrix, Inc.. The 510(k) number is K240424.

When was Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix approved by the FDA?

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

What company makes Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix?

Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix is manufactured by Collagen Matrix, Inc..

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.