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FDA 510(k)

UroLift System (UL400 and UL500)

K-Number: K173087 · 2017-12-28

Decision Date2017-12-28
Product CodePEW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UroLift System (UL400 and UL500) is a medical device manufactured by Neotract, Inc.. It received FDA 510(k) clearance on 2017-12-28 under approval number K173087. The device is classified under product code PEW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UroLift System (UL400 and UL500)?

UroLift System (UL400 and UL500) is a medical device that received FDA 510(k) clearance on 2017-12-28. It is manufactured by Neotract, Inc.. The 510(k) number is K173087.

When was UroLift System (UL400 and UL500) approved by the FDA?

UroLift System (UL400 and UL500) received FDA 510(k) clearance on 2017-12-28, under approval number K173087.

What company makes UroLift System (UL400 and UL500)?

UroLift System (UL400 and UL500) is manufactured by Neotract, Inc..

What is the FDA product code for UroLift System (UL400 and UL500)?

The FDA product code for UroLift System (UL400 and UL500) is PEW.

Other Devices by Neotract, Inc.

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Related Devices (Code: PEW)

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.