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: ILZ FDA class 1

Accessories, Traction

Physical Medicine

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Traction Accessories are supplementary components used with physical medicine traction devices, including harnesses, spreader bars, pulleys, and weights that form part of a mechanical traction system used to apply stretching forces to the spine or limbs for pain relief and musculoskeletal treatment. It is classified as FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. The product code is ILZ, regulated under 21 CFR 890.5925, within the Physical Medicine medical specialty. This device is GMP exempt, indicating it is not subject to full good manufacturing practice requirements.

510(k) Clearances

15 matches
K Number
Device Name
FLEXION DISTRATION SUPPORT
VIBRA-TRAC TRACTION TABLE
AMX-110, AMX-II AND AMX-III
VECTOR BAR SUSPENSION/TRACTION UNIT
TRACTION ACCESSORIES
SAUNDERS #7080 CERVICAL TRACTION SYS
HEAD HALTER
PELVIC TRACTION BELT
PELVIC TRACTION BELT
BOGER AUTO-TRACTION DEVICE
CERVI-TRAC
BANDAGE SPREADER BLOCK
TRACTION BELT, PELVIC
SPREADER BARS
TRACTION HARNESS

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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