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: NWF FDA class 1

Drill, Battery Powered, Subungual Hematoma

General, Plastic Surgery

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The Battery-Powered Subungual Hematoma Drill is a surgical tool intended to cut a hole in finger or toenails to release fluid accumulated in the underlying nail bed, relieving pressure from subungual hematomas including black toe injuries. It provides a controlled, powered method for nail trephination without the need for heat-based devices. It is an FDA Class 1 device regulated under 21 CFR 878.4820 in the General and Plastic Surgery specialty, with product code NWF, and is exempt from premarket notification under submission type 4. It does not carry implant or life-sustaining support designations.

510(k) Clearances

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Device Name
PATHFORMER

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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