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FDA 510(k)

Mineral Collagen Composite Bioactive Extra Moldable

K-Number: K231942 · 2023-08-02

ApplicantCollagen Matrix, Inc.
Decision Date2023-08-02
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Mineral Collagen Composite Bioactive Extra Moldable 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 2023-08-02 under 510(k) 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. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K231942.

When did Mineral Collagen Composite Bioactive Extra Moldable receive FDA 510(k) clearance?

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

Who is the listed applicant for Mineral Collagen Composite Bioactive Extra Moldable?

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 Extra Moldable?

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

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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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