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FDA 510(k)

Forcyte Autograft Harvest Kit

N.º K: K243407 · 2025-07-29

SolicitanteForcyte Medical, LLC
Fecha de decisión2025-07-29
Código de productoKNW
Comité asesorGU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Forcyte Autograft Harvest Kit is the device name listed in this FDA 510(k) record. The listed applicant is Forcyte Medical, LLC. It received FDA 510(k) clearance on 2025-07-29 under 510(k) number K243407. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Forcyte Autograft Harvest Kit?

Forcyte Autograft Harvest Kit is a medical device that received FDA 510(k) clearance on 2025-07-29. The listed applicant is Forcyte Medical, LLC. The 510(k) number is K243407.

When did Forcyte Autograft Harvest Kit receive FDA 510(k) clearance?

Forcyte Autograft Harvest Kit received FDA 510(k) clearance on 2025-07-29, under 510(k) number K243407.

Who is the listed applicant for Forcyte Autograft Harvest Kit?

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

What is the FDA product code for Forcyte Autograft Harvest Kit?

The FDA product code for Forcyte Autograft Harvest Kit is KNW.

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Fuente oficial

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