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.

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Product Code: LBK FDA unclassified

Neurosurgical Ultrasonic Instruments

Unknown

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Neurosurgical ultrasonic instruments are devices used in neurosurgery to fragment and aspirate tissue, such as brain tumors, using high-frequency ultrasonic energy. This device type is currently unclassified by the FDA, meaning it has not been assigned a definitive risk class and its regulatory requirements remain under evaluation. The product code is LBK, with no regulation number or medical specialty formally assigned. No special risk flags apply.

510(k) Clearances

7 matches
K Number
Device Name
DISSECTRON PORTABLE UNIT
OLYMPUS ULTRASONIC SURGICAL SYSTEM (USU)
CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR
CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA.
AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT
BOVIE ULTRASONIC SURGICAL SYSTEM
COOPER LASER SONICS CUSA MODEL 200

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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