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: FYH FDA class 1

Splint, Extremity, Noninflatable, External, Sterile

General, Plastic Surgery

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A sterile noninflatable external extremity splint is a rigid or semi-rigid support device applied externally to an injured limb to immobilize and protect fractures, dislocations, or soft tissue injuries, supplied in a sterile condition. It is classified as FDA Class 1 (lowest risk), subject to general controls only, and does not require premarket notification. The product code is FYH, regulated under 21 CFR 878.3910, within the General, Plastic Surgery medical specialty. No special flags apply to this device.

510(k) Clearances

8 matches
K Number
Device Name
TRACE MODEL #'S 840, 841, 842, 845
SPECIALIST(R) WALKER
KUT-SHIELD
SPLINTS(ALL TYPE)
HYDRO-SPLINT A SPONGE-COMPRESS DRESS
J & J DIP WATER ADDITIVE
DELTA-LITE CASTING TAPE & SPLINTS
ORTHOPEDIC LOWER EXTREMITY SUSPENSION

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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