FDA 510(k)

GIA Stapler with Tri-Staple Technology

N.º K: K202701 · 2020-12-07

Fecha de decisión2020-12-07

Código de productoGDW

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

GIA Stapler with Tri-Staple Technology is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2020-12-07 under 510(k) number K202701. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the GIA Stapler with Tri-Staple Technology?

GIA Stapler with Tri-Staple Technology is a medical device that received FDA 510(k) clearance on 2020-12-07. The listed applicant is Covidien. The 510(k) number is K202701.

When did GIA Stapler with Tri-Staple Technology receive FDA 510(k) clearance?

GIA Stapler with Tri-Staple Technology received FDA 510(k) clearance on 2020-12-07, under 510(k) number K202701.

Who is the listed applicant for GIA Stapler with Tri-Staple Technology?

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

What is the FDA product code for GIA Stapler with Tri-Staple Technology?

The FDA product code for GIA Stapler with Tri-Staple Technology is GDW.

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Fuente oficial

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