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: ITQ FDA class 1

Joint, Knee, External Brace

Physical Medicine

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A knee joint external brace component is an articulating joint unit incorporated into knee orthoses to allow controlled flexion and extension while providing structural support and stability to the knee. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is ITQ, regulated under 21 CFR 890.3475, within the Physical Medicine medical specialty. This device is GMP exempt.

510(k) Clearances

15 matches
K Number
Device Name
LIMITED MOTION FUNCTIONAL KNEE BRACE
BRACE C.T.
DELUXE KNEE IMMOBILIZER(UNIVERSAL)
ANATOMIC FRACTURE BRACE
DELUXE KNEE IMMOBILIZER
NEOPRENE KNEE SUPPORT
AIRCAST PNEUMATIC KNEE BRACE
CYLINDER KNEE CAST/SPLINT
LIMB ORHTOSIS
KNEE BRACE/STABILIZER
FRACTURE BRACING
SETUP WALKER ADJUSTABLE
DEMI-WALKER (REGULAR)
SETUP WALKER OVER TOILET CONSTRUC.
WALKER FOLDING ADJUSTABLE

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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