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: GAS FDA class 2

Suture, Nonabsorbable, Synthetic, Polyester

General, Plastic Surgery

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The Suture, Nonabsorbable, Synthetic, Polyester (product code GAS) is a durable synthetic suture made from polyester material, used in general and plastic surgery for applications requiring permanent or long-lasting tissue support, such as cardiac, vascular, or orthopedic procedures. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. 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 embedded within body tissue.

510(k) Clearances

17 matches
K Number
Device Name
RD QUICK LOAD SUTURE, 0 Polyester, RD QUICK LOAD SUTURE, 2-0 Polyester, RD QUCIK LOAD SUTURE, 2-0 Polypropylene
RAM COR-SUTURE QUCIK LOAD Surgical Suture, COR-SUTURE QUICK LOAD Surgical Suture
ARTHREX BIOWIRE
MR-III
SUTURE CORD
BRAIDED POLYESTER SUTURE MATERIAL
PETERS CARDIOFLON(TM) SUTURE
MITEK QUICKANCHOR(TM), MODIFICATION
MITEK SNAP PAK(TM), MODIFICATION
ADVANCE SUTURE NONABSORBABLE DACRON SUTURE
IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES
FINE SIZE NONABSORBABLE DACRON SURGICAL SUTURE
LU-TEX II
QUICKANCHOR (TM)
DACRON R SURGICAL SUTURES
POLYVIOLENE(TM) SUTURE
NONABSORBABLE DACRON SURGICAL SUTURE*

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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