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: INP FDA class 1

Tips And Pads, Cane, Crutch And Walker

Physical Medicine

View full classification →

Tips and Pads for Canes, Crutches, and Walkers are replacement or accessory components attached to the bottom of walking aids to improve grip and traction on surfaces, reduce shock transmission, and protect floors, used in Physical Medicine to enhance safety and comfort for ambulatory patients with mobility impairments. It is classified as FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. The product code is INP, regulated under 21 CFR 890.3790, within the Physical Medicine medical specialty. This device is GMP exempt, indicating it is not subject to full good manufacturing practice requirements.

510(k) Clearances

8 matches
K Number
Device Name
SURGEON'S CHOICE CRUTCH HANDLE
PERSONAL KNEE CRUTCH PAD
CRUTCH & WALKER PADS
CRUTCH TIPS & GRIPS
CONPHAR CRUTCH GRIPS
CONPHAR CRUTCH TIPS
CONPHAR CRUTCH PADS
CRUTCH TIPS, PADS & HAND GRIPS

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.

Popular Product Codes

Commonly searched