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FDA 510(k)

Mineral Collagen Composite Bioactive Extra Moldable

K-Number: K231942 · 2023-08-02

Decision Date2023-08-02
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Mineral Collagen Composite Bioactive Extra Moldable is a medical device manufactured by Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2023-08-02 under approval number K231942. 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 Extra Moldable?

Mineral Collagen Composite Bioactive Extra Moldable is a medical device that received FDA 510(k) clearance on 2023-08-02. It is manufactured by Collagen Matrix, Inc.. The 510(k) number is K231942.

When was Mineral Collagen Composite Bioactive Extra Moldable approved by the FDA?

Mineral Collagen Composite Bioactive Extra Moldable received FDA 510(k) clearance on 2023-08-02, under approval number K231942.

What company makes Mineral Collagen Composite Bioactive Extra Moldable?

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

What is the FDA product code for Mineral Collagen Composite Bioactive Extra Moldable?

The FDA product code for Mineral Collagen Composite Bioactive Extra Moldable 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.