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: HCF FDA class 1

Instrument, Ligature Passing And Knot Tying

General, Plastic Surgery

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The Ligature Passing and Knot Tying Instrument is a surgical tool used in general and plastic surgery to pass suture material around structures and to tie secure knots in confined or deep anatomical spaces where direct manual tying is difficult. It is classified as a Class 1 device (lowest risk), subject to general controls only. The product code is HCF under regulation 21 CFR 878.4800 in the General, Plastic Surgery specialty. No implant, life-sustaining, GMP exempt, or third-party review flags apply.

510(k) Clearances

5 matches
K Number
Device Name
Edwards Suture Fastening System
MICROVASIVE INSURG LAPTIE SUTURE LIGATOR
VALTRAC PURSESTING DEVICE
STROVER HOOK
HEMORRHOIDAL LIGATOR

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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