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: HXJ FDA class 1

Staple Driver

Orthopedic

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A staple driver is a handheld orthopedic instrument used to insert bone staples into bone tissue for fracture fixation, epiphysiodesis, or soft tissue reattachment. It is classified as an FDA Class 1 device under 21 CFR 888.4540, indicating minimal risk subject to general controls. Product code HXJ falls under the Orthopedic medical specialty.

510(k) Clearances

6 matches
K Number
Device Name
IN-TAC BONE ANCHOR SYSTEM
UROTAC BONE ANCHOR INSERTER
ELECTRIC WIRE DRIVER, MODEL 2640E
FIXATION STAPLE KIT - DLIDE HAMMER
OSTEOTOMY BONE STAPLE
STAPLE INSERTER-EXTRACTOR FOR ARTHROS

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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