Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: PEW FDA class 2

Implantable Transprostatic Tissue Retractor System

Gastroenterology, Urology

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The Implantable Transprostatic Tissue Retractor System is a urology device indicated for the treatment of lower urinary tract symptoms due to urinary outflow obstruction secondary to benign prostatic hyperplasia (BPH) in men aged 45 years or older, using a minimally invasive approach to retract obstructing prostatic tissue. It falls under the Gastroenterology and Urology medical specialty and is classified as a Class 2 device under regulation 876.5530, requiring 510(k) premarket notification. As an implant, it is subject to general controls and special controls; it is not considered life-sustaining.

510(k) Clearances

11 matches
K Number
Device Name
UroLift 2 ATC Advanced Tissue Control System
UroLift 2 System (formerly UL500), UroLift 2 Delivery Handle, UroLift 2 Implant Cartridge
UroLift Advanced Tissue Control (ATC) System
UroLift System (UL400)
UroLift System UL400
UroLift System (UL400 and UL500)
UroLift System (UL500)
UroLift System UL500, UroLift Delivery Handle, UroLift Implant Cartiridge
NeoTract UroLift System UL500
NEOTRACT UROLIFT SYSTEM
UROLIFT SYSTEM

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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