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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

Free to try · every answer cites its records

Product Code: IQF FDA class 1

Orthosis, Cervical-Thoracic, Rigid

Physical Medicine

View full classification →

A rigid cervical-thoracic orthosis is a firm external brace extending from the neck through the upper thoracic spine, used to immobilize and support the cervicothoracic junction following injury or surgery. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is IQF, regulated under 21 CFR 890.3490, within the Physical Medicine medical specialty. This device is GMP exempt.

510(k) Clearances

7 matches
K Number
Device Name
JASON CERVICAL ORTHOSIS
ZEE EXTRICATION DEVICE
CERVICAL SUPPORT
SCOLIOSIS ORTHOTIC SYSTEM
POPE AMBULATORY HALO VEST
KENDRICK EXTRICATION DEVICE
SPINE BOARD

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.

Popular Product Codes

Commonly searched