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FDA 510(k)

EsophyX Z+ Device with SerosaFuse Fasteners and Accessories

K-Number: K240879 · 2024-04-26

Decision Date2024-04-26
Product CodeODE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EsophyX Z+ Device with SerosaFuse Fasteners and Accessories is a medical device manufactured by Endogastric Solutions, Inc.. It received FDA 510(k) clearance on 2024-04-26 under approval number K240879. The device is classified under product code ODE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EsophyX Z+ Device with SerosaFuse Fasteners and Accessories?

EsophyX Z+ Device with SerosaFuse Fasteners and Accessories is a medical device that received FDA 510(k) clearance on 2024-04-26. It is manufactured by Endogastric Solutions, Inc.. The 510(k) number is K240879.

When was EsophyX Z+ Device with SerosaFuse Fasteners and Accessories approved by the FDA?

EsophyX Z+ Device with SerosaFuse Fasteners and Accessories received FDA 510(k) clearance on 2024-04-26, under approval number K240879.

What company makes EsophyX Z+ Device with SerosaFuse Fasteners and Accessories?

EsophyX Z+ Device with SerosaFuse Fasteners and Accessories is manufactured by Endogastric Solutions, Inc..

What is the FDA product code for EsophyX Z+ Device with SerosaFuse Fasteners and Accessories?

The FDA product code for EsophyX Z+ Device with SerosaFuse Fasteners and Accessories is ODE.

Other Devices by Endogastric Solutions, Inc.

Related Devices (Code: ODE)

Official Source

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