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: ONN FDA class 2

Intraoperative Orthopedic Joint Assessment Aid

Neurology

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The Intraoperative Orthopedic Joint Assessment Aid (product code ONN) is a Class 2 device regulated under 21 CFR 882.4560, reviewed by the Orthopedic panel in the Neurology specialty classification (NE), cleared via 510(k). It is intended for the intraoperative measurement and interpretation of orthopedic joint information to assist surgeons during joint procedures. The device is not an implant and is not life-sustaining.

510(k) Clearances

15 matches
K Number
Device Name
QUADSENSE
Lantern® Hip
TrueBalance™ Surgical System
VERASENSE for Exactech Equinoxe Size 38 mm, VERASENSE for Exactech Equinoxe Size 42 mm, LinkStation MINI, LinkStation MINI Evaluation Kit, VERASENSE Software Application for Shoulder
VERASENSE for Stryker Triathlon
VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left
VERASENSE for Zimmer Biomet Persona
XO1 Knee Balancing System
VERASENSE Knee System
ELIBRA SOFT-TISSUE FORCE SENSOR
ORTHOSENSOR KNEE BALANCER, VERASENSE KNEE SYSTEM
ORTHOSENSOR KNEE BALANCER
ELIBRA UNI SOFT-TISSUE FORCE SENSOR, MODEL 61-XXXX(5 MODELS, DIFFERENT SIZES
ORTHOREX INTRA-OPERATIVE LOAD SENSOR
ELIBRA DYNAMIC KNEE BALANCER

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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