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: IPY FDA class 1

Orthosis, Lumbo-Sacral

Physical Medicine

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A lumbo-sacral orthosis is an external brace encompassing the lumbar spine and sacral region, used to provide support, limit motion, and relieve pain in the lower back. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is IPY, regulated under 21 CFR 890.3490, within the Physical Medicine medical specialty. This device is GMP exempt.

510(k) Clearances

11 matches
K Number
Device Name
M-BRACE
LUMBOSACRAL SUPPORT
CUSTOM CONTOUR LUMBOSACRAL ORTHOSIS
CASH ORTHOSIS
LUMBO-SACRAL FLEXION ORTHOSIS
SPINAL EXTENSION BRACE
LUMBAR FLEXION BRACE
CRUSADER HYPEREXTENSION BRACE
LUMBOSACRAL SUPPORTS & THORACO-LUMBO-SAC
WRIGHT DOW CORNING SOFTGOODS W/DOW
VERTEBRACE SPINAL SUPPORTS

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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