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: GAT FDA class 2

Suture, Nonabsorbable, Synthetic, Polyethylene

General, Plastic Surgery

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The Suture, Nonabsorbable, Synthetic, Polyethylene (product code GAT) is a synthetic, nonabsorbable suture constructed from polyethylene, used in general and plastic surgery to provide lasting wound closure and tissue approximation where permanent suture material is indicated. It is classified as FDA Class 2, requiring a 510(k) premarket notification to demonstrate substantial equivalence. The device is regulated under 21 CFR 878.5000 in the General, Plastic Surgery specialty (SU). This device carries an implant designation, as it is placed through body tissue during application.

510(k) Clearances

50+ matches
K Number
Device Name
HyperSuture White/Green Extension Line
HyperSuture All Blue Extension Line
HyperSuture Extension Line
HS Fiber Sutures
HyperSuture
Non absorbable Surgical Polyester Suture
SuperBall Meniscal Repair System
MENIX®; MENIX® DUO
MyEllevate
AceConnex Pre-Sutured Fascia
Pre-Sutured Tendon (4561SC / Single Strand); Pre-Sutured Tendon (4564SC / Quadruple Strand )
ACTIVBRAID™
Arthrex BioSuture
Arthrex SoftStitch
Arthrex SutureTape
Zone Specific AIM
PERMALOOP Suture, PERMATAPE Suture
Arthrex LoopLoc Knotless Suture
EasyWhip
DYNATAPE Suture
FAST-FIX FLEX
Arthrex SoftStitch
HS Fiber
Arthrex SutureTape
Tevdek II, Silky II Polydek, 'Cottony' II, NextStitch
High Strength Suture
DemeTECH DemeFORCE Nonabsorbable Surgical Suture
Force Fiber Suture
HS Fiber
MTF Pre-Sutured Tendon
Force Fiber White and White/Blue, White/Black, Blue, and White/Green sutures; Force Fiber OrthoTape suture; Bondek suture and Bondek Plus suture; Monodek suture; Polyglytone*6211 suture
DYNACORD Suture
NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0)
SuperBall Meniscal Repair System
NovoStitch Pro Meniscal Repair System
ReConnex Pre-Sutured Tendon
Force Fiber Fusion Suture
GRAVITY™ Soft Tissue Repair System
Infinity-Lock 3, Infinity-Lock 5
SutureTape
ExpressBraid Graft Manipulation
SpeedStitch Suture Passer; SpeedStitch Suture Cartridges, White Suture, Blue Cobraid, Black Cobraid, Mixed Pack; SpeedStitch Needle Loader and Unloader
MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture
PERMATAPE
XBraid TT Suture Tape
SPEEDTRAP Graft Preparation System
'cottony' II TAPE, PLEDGETS
IvyAIR Meniscus System, Curved, IvyAIR Meniscus System, Straight, IvyAIR Meniscus System, Reverse Curved
silky II POLYDEK, cottony II, TEVDEK II, NextStitch, DEKLENE II, DEKLENE MAXX Gabbay-Frater, NYLON, SILK, STAINLESS STEEL
Dunamis Force DFX Tensile Tape

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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