FDA 510(k)

Porous Biologic Scaffold

Número K: K240765 · 2024-12-18

Data da decisão2024-12-18

Código do produtoMQV

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Porous Biologic Scaffold is the device name listed in this FDA 510(k) record. The listed applicant is Ventris Medical. It received FDA 510(k) clearance on 2024-12-18 under 510(k) number K240765. 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 Porous Biologic Scaffold?

Porous Biologic Scaffold is a medical device that received FDA 510(k) clearance on 2024-12-18. The listed applicant is Ventris Medical. The 510(k) number is K240765.

When did Porous Biologic Scaffold receive FDA 510(k) clearance?

Porous Biologic Scaffold received FDA 510(k) clearance on 2024-12-18, under 510(k) number K240765.

Who is the listed applicant for Porous Biologic Scaffold?

The FDA 510(k) record lists Ventris Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Porous Biologic Scaffold?

The FDA product code for Porous Biologic Scaffold is MQV.

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Fonte oficial

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