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FDA 510(k)

EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil

K-Number: K232126 · 2023-08-16

ApplicantCovidien
Decision Date2023-08-16
Product CodeGAG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil is a medical device manufactured by Covidien. It received FDA 510(k) clearance on 2023-08-16 under approval number K232126. 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 EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil?

EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil is a medical device that received FDA 510(k) clearance on 2023-08-16. It is manufactured by Covidien. The 510(k) number is K232126.

When was EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil approved by the FDA?

EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil received FDA 510(k) clearance on 2023-08-16, under approval number K232126.

What company makes EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil?

EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil is manufactured by Covidien.

What is the FDA product code for EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil?

The FDA product code for EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil is GAG.

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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.