FDA 510(k)

Endoform Plastics and Reconstructive Matrix

N.º K: K162461 · 2016-12-20

SolicitanteAroa Biosurgery (Formerly Mesynthes Limited)

Fecha de decisión2016-12-20

Código de productoFTM

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Endoform Plastics and Reconstructive Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Aroa Biosurgery (Formerly Mesynthes Limited). It received FDA 510(k) clearance on 2016-12-20 under 510(k) number K162461. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Endoform Plastics and Reconstructive Matrix?

Endoform Plastics and Reconstructive Matrix is a medical device that received FDA 510(k) clearance on 2016-12-20. The listed applicant is Aroa Biosurgery (Formerly Mesynthes Limited). The 510(k) number is K162461.

When did Endoform Plastics and Reconstructive Matrix receive FDA 510(k) clearance?

Endoform Plastics and Reconstructive Matrix received FDA 510(k) clearance on 2016-12-20, under 510(k) number K162461.

Who is the listed applicant for Endoform Plastics and Reconstructive Matrix?

The FDA 510(k) record lists Aroa Biosurgery (Formerly Mesynthes Limited) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Endoform Plastics and Reconstructive Matrix?

The FDA product code for Endoform Plastics and Reconstructive Matrix is FTM.

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Dispositivos relacionados (Código: FTM)

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Fuente oficial

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