FDA 510(k)

NovaBone Putty - Synthetic Bioactive Bone Graft

N.º K: K242299 · 2024-09-25

Fecha de decisión2024-09-25

Código de productoMQV

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

NovaBone Putty - Synthetic Bioactive Bone Graft is the device name listed in this FDA 510(k) record. The listed applicant is Novabone Products, LLC. It received FDA 510(k) clearance on 2024-09-25 under 510(k) number K242299. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the NovaBone Putty - Synthetic Bioactive Bone Graft?

NovaBone Putty - Synthetic Bioactive Bone Graft is a medical device that received FDA 510(k) clearance on 2024-09-25. The listed applicant is Novabone Products, LLC. The 510(k) number is K242299.

When did NovaBone Putty - Synthetic Bioactive Bone Graft receive FDA 510(k) clearance?

NovaBone Putty - Synthetic Bioactive Bone Graft received FDA 510(k) clearance on 2024-09-25, under 510(k) number K242299.

Who is the listed applicant for NovaBone Putty - Synthetic Bioactive Bone Graft?

The FDA 510(k) record lists Novabone Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NovaBone Putty - Synthetic Bioactive Bone Graft?

The FDA product code for NovaBone Putty - Synthetic Bioactive Bone Graft is MQV.

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Otros registros que enlistan a Novabone Products, LLC como solicitante

K240404NovaBone Putty - Bioactive Synthetic Bone Graft (NB6600, NB6610, NB6615)K220498NovoGen Wound Matrix K163310NovaBone IRM

Dispositivos relacionados (Código: MQV)

Fuente oficial

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