FDA 510(k)

Mineral Collagen Composite Bioactive Moldable

Número K: K221735 · 2022-12-20

Data da decisão2022-12-20

Código do produtoMQV

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Mineral Collagen Composite Bioactive 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 2022-12-20 under 510(k) number K221735. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

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. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K221735.

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

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

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

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

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Fonte oficial

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