FDA 510(k)

Synthetic Bone Putty

Número K: K221644 · 2022-09-02

Data da decisão2022-09-02

Código do produtoMQV

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Synthetic Bone Putty is the device name listed in this FDA 510(k) record. The listed applicant is Ventris Medical. It received FDA 510(k) clearance on 2022-09-02 under 510(k) number K221644. 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 Synthetic Bone Putty?

Synthetic Bone Putty is a medical device that received FDA 510(k) clearance on 2022-09-02. The listed applicant is Ventris Medical. The 510(k) number is K221644.

When did Synthetic Bone Putty receive FDA 510(k) clearance?

Synthetic Bone Putty received FDA 510(k) clearance on 2022-09-02, under 510(k) number K221644.

Who is the listed applicant for Synthetic Bone Putty?

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 Synthetic Bone Putty?

The FDA product code for Synthetic Bone Putty is MQV.

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Fonte oficial

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