FDA 510(k)

GIA Stapler with Tri-Staple Technology

K-Number: K231934 · 2023-10-27

Decision Date2023-10-27

Product CodeGAG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

GIA Stapler with Tri-Staple Technology is a medical device manufactured by Covidien. It received FDA 510(k) clearance on 2023-10-27 under approval number K231934. The device is classified under product code GAG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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 2023-10-27. It is manufactured by Covidien. The 510(k) number is K231934.

When was GIA Stapler with Tri-Staple Technology approved by the FDA?

GIA Stapler with Tri-Staple Technology received FDA 510(k) clearance on 2023-10-27, under approval number K231934.

What company makes GIA Stapler with Tri-Staple Technology?

GIA Stapler with Tri-Staple Technology is manufactured by Covidien.

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 GAG.

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Related Devices (Code: GAG)

K213633ECHELON 3000 45mm Stapler, ECHELON 3000 60mm StaplerEthicon Endo-Surgery, LLC K231491TA Stapler and Loading Unit with DST Series TechnologyCovidien K232126EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler AnvilCovidien K221629Tri-Staple 2.0 Black Circular Reloads (for use with Signia Circular Adapters)Covidien K240881Signia Circular Adapter (Standard Length) (SIGCIRSTND); Signia Circular Adapter XL Length (SIGCIRXL)Covidien (Part of Medtronic) K241629ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm Standard Stapler (ECH45S); Echelon 3000 45mm Long Stapler (ECH45L); Echelon 3000 60mm Compact Stapler (ECH60C); Echelon 3000 60mm Standard Stapler (ECH60S); Echelon 3000 60mm Long Stapler (ECH60L)Ethicon Endo-Surgery, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.