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: JEA FDA class 1

Table, Surgical With Orthopedic Accessories, Ac-Powered

General, Plastic Surgery

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The AC-Powered Surgical Table with Orthopedic Accessories is an electrically powered operating table designed to position patients during orthopedic surgical procedures, accommodating traction, limb support, and specialized attachment devices. It is classified as FDA Class 1 (lowest risk), subject only to general controls including registration and proper labeling. The product code is JEA, regulated under 21 CFR 878.4960, within the General and Plastic Surgery medical specialty. No special flags apply to this device.

510(k) Clearances

10 matches
K Number
Device Name
STRYKER COMMAND2 OFFICE CONSOLE
MEND APC
JACKSON MULTIPURPOSE OPERATING TABLE
ARTHROBOT(TM) WRIST HOLDER ACCESSORY
SKYTRON MODEL 1100 AND MODEL 142
DMI 250 SERIES POWER SURGERY TABLE
OSI RIZZOLI TRAUMA TABLE (ELECTRIC VERSION)
ARTHROTRACT UPPER LIMB TRACTION ACCESSORY
ARTHROBOT 100 UPPER LIMB POSITIONER
ARTHROBOT 101 UPPER LIMB TRACTION ACCESSORY

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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