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: GZX FDA class 1

Instrument, Microsurgical

Neurology

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The Microsurgical Instrument is a precision hand-held tool used in neurosurgical procedures performed under magnification, including delicate dissection, manipulation, and tissue handling in procedures on the brain, spinal cord, and peripheral nerves. It is classified as a Class 1 device (lowest risk), subject to general controls only, reflecting its basic mechanical nature. The product code is GZX under regulation 21 CFR 882.4525 in the Neurology specialty. No implant, life-sustaining, GMP exempt, or third-party review flags apply.

510(k) Clearances

13 matches
K Number
Device Name
MICROSURGICAL INSTRUMENTS
CLARUS ENDOSCOPIC BALL PROBE
J105 JAMES SURGICAL SYSTEM I/A PACK
MICROSURGICAL KERATOME
RANGE OF NEUROSURGICAL INSTRUMENTS IN TITANIUM
RANGE OF CROCODILE ACTION INSTRUMENTS
MICRA MICROSURGICAL INSTRUMENTS
THE VICKERS STANDARD MICROSURGERY SET
VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND
VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED
VICKERS ERGOMATIC MICROS INSTR-FINE R OR L HANDED
UNIVERSAL INSTRU. SET FOR NEUROVASCULAR
DUJOVNY MICROSURGICAL SCISSORS

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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