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.

Product Code: PNO FDA class 2

Catheter, Percutaneous, Cutting/Scoring

Cardiovascular

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The Catheter, Percutaneous, Cutting/Scoring (product code PNO) is a Class 2 cardiovascular device intended to reduce vascular stenosis by dilatation and apposition of cutting or scoring surfaces to stenotic material within the vasculature, regulated under 870.1250. It requires 510(k) clearance and falls under the cardiovascular medical specialty. The device is not an implant and is not life-sustaining.

510(k) Clearances

44 matches
K Number
Device Name
Aperta NSE PTA Balloon Dilatation Catheter
D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter
Tri-Wedge PTA Scoring Balloon Dilatation Catheter
XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter
Aperta NSE PTA Balloon Dilatation Catheter (AW18-05040040/AA18-05040040, AW18-09040040/AA18-09040040, AW18-14540040, AW18-05050040/AA18-05050040, AW18-09050040/AA18-09050040, AW18-14550040, AW18-05060040/AA18-05060040, AW18-09060040/AA18-09060040, AW18-14560040 AW18-05070040/AA18-05070040, AW18-09070040/AA18-09070040, AW18-14570040, AW18-05080040/AA18-05080040, AW18-09080040/AA18-09080040, AW18-14580040)
D·Kutting™ PTA Scoring Balloon Dilatation Catheter
XO Score LP Percutaneous Transluminal Angioplasty Scoring Catheter, XO Score LP Catheter
Serranator PTA Serration Balloon Catheter
Serranator PTA Serration Balloon Catheter
Serranator PTA Serration Balloon Catheter
FLEX Vessel Prep System
XO Score Percutaneous Transluminal Angioplasty Scoring Catheter
Serranator PTA Serration Balloon Catheter
Scoreflex PTA Scoring Balloon Catheter
ULTRASCORE Focused Force PTA Balloon
UltraScore Focused Force PTA Balloon
Serranator Alto PTA Serration Balloon Catheter
FLEX SCORING CATHETER
2cm Peripheral Cutting Balloon Microsurgical Dilatation Catheter
AngioSculpt PTA Scoring Baloon Catheters
ADVANCE ENFORCER 35 FOCAL FORCE PTA BALLOON CATHETER
AngioSculpt PTA Scoring Balloon Catheter with HydroCross Coating
ANGIOSCULPT PTA SCORING BALLOON WITH HYDROCROSS CAOTING
ANGIOSCULPT PTA SCORING BALLOON CATHETER
SPLITWIRE PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY SCORING DEVICE
ANGIOSCULPT PTA SCORING BALLOON CATHETER
ANGIOSCULPT PTA SCORING BALLOON CATHETER
VASCUTRAK PTA DILATATION CATHETER
ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2155-XXYY
ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2076-XXYY, 2092-XXYY, 2105-XXYY
ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076-6040, 2092-6040, 2105-6040
VASCUTRAK 2, MODELS: V14 AND V18
ANGIOSCULPT PTA SCORING BALLOON CATHETER
MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER
ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076 AND 2039
VASCUTRAK II PTA DILATATION CATHETER
ANGIOSCULPT PTA SCORING BALLOON CATHETER
2CM PERIPHERAL CUTTING BALLOON, SMALL PERIPHERAL CUTTING BALLOON WITH MONORAIL AND OVER-THE-WIRE DELIVERY SYSTEMS
VASCUTRAK PTA DILATION CATHETER
SMALL PERIPHERAL CUTTING BALLON, MONORAIL DELIVERY SYSTEM
ANGIOSCULPT SCORING BALLOON CATHETER
PERIPHERAL CUTTING BALLOON
2 CM PERIPHERAL CUTTING BALOON
PERIPHERAL CUTTING BALLOON

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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