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FDA 510(k)

Mineral Collagen Composite Bioactive Moldable

K-Number: K221735 · 2022-12-20

ApplicantCollagen Matrix, Inc.
Decision Date2022-12-20
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Mineral Collagen Composite Bioactive Moldable is a medical device manufactured by Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2022-12-20 under approval number K221735. 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?

Mineral Collagen Composite Bioactive Moldable is a medical device that received FDA 510(k) clearance on 2022-12-20. It is manufactured by Collagen Matrix, Inc.. The 510(k) number is K221735.

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

Mineral Collagen Composite Bioactive Moldable received FDA 510(k) clearance on 2022-12-20, under approval number K221735.

What company makes Mineral Collagen Composite Bioactive Moldable?

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

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

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

Related Clinical Trials

NCT07598305 PICN Versus Bioactive Composite for Cervical Restorations in Ballet Dancers COMPLETED NCT07580495 Effect of Collagen Membrane on Ridge Preservation NOT_YET_RECRUITING NCT07524842 Clinical Performance of Three Different Restorative Materials NOT_YET_RECRUITING NCT07547904 Clinical Performance of Bioactive Bulk-Fill in Class II Restorations RECRUITING

Other Devices by Collagen Matrix, Inc.

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Official Source

View on FDA Database →

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

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