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: HTW FDA class 1

Bit, Drill

Orthopedic

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A drill bit is a rotary cutting tool used in orthopedic surgery to create holes in bone for the placement of screws, pins, wires, or other fixation hardware. It is classified as an FDA Class 1 device under 21 CFR 888.4540, indicating low risk and general controls only. Product code HTW falls under the Orthopedic medical specialty.

510(k) Clearances

11 matches
K Number
Device Name
Renovo Life Hard Carbon Coated Drill Bit
AGEE-WRISTJACK PRE-DRILL KIT
REAMER BIT
CANNULATED DRILL BIT
MITEK ANCHOR DRILL
FEMORAL CEMENT REMOVAL INSTRUMENTS
GLENOID DRILL
DRILL BIT
BONE PLUGGING TOOL
SURGICAL DRILL BITS
UNIVERSALL DRILL GUIDE

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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