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FDA 510(k)

NEOTRACT UROLIFT SYSTEM

K-Number: K133281 · 2013-12-20

ApplicantNeotract, Inc.
Decision Date2013-12-20
Product CodePEW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEOTRACT UROLIFT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Neotract, Inc.. It received FDA 510(k) clearance on 2013-12-20 under 510(k) number K133281. 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 NEOTRACT UROLIFT SYSTEM?

NEOTRACT UROLIFT SYSTEM is a medical device that received FDA 510(k) clearance on 2013-12-20. The listed applicant is Neotract, Inc.. The 510(k) number is K133281.

When did NEOTRACT UROLIFT SYSTEM receive FDA 510(k) clearance?

NEOTRACT UROLIFT SYSTEM received FDA 510(k) clearance on 2013-12-20, under 510(k) number K133281.

Who is the listed applicant for NEOTRACT UROLIFT SYSTEM?

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

What is the FDA product code for NEOTRACT UROLIFT SYSTEM?

The FDA product code for NEOTRACT UROLIFT SYSTEM is PEW.

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Other records listing Neotract, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K232558UroLift 2 ATC Advanced Tissue Control SystemK212396UroLift System Rigid Retrieval Kit Sterilization TrayK201837UroLift 2 System (formerly UL500), UroLift 2 Delivery Handle, UroLift 2 Implant CartridgeK200441UroLift Advanced Tissue Control (ATC) SystemK192781UroLift System Procedure Kit Sterilization TrayK193269UroLift System (UL400)

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Related Devices (Code: PEW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K232558UroLift 2 ATC Advanced Tissue Control SystemNeotract, Inc.K201837UroLift 2 System (formerly UL500), UroLift 2 Delivery Handle, UroLift 2 Implant CartridgeNeotract, Inc.K200441UroLift Advanced Tissue Control (ATC) SystemNeotract, Inc.K193269UroLift System (UL400)Neotract, Inc.K190377UroLift System UL400Neotract, Inc.K173087UroLift System (UL400 and UL500)Neotract, Inc.

Official Source

View on FDA Database →

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

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