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: HTP FDA class 1

File

Orthopedic

View full classification →

An orthopedic file is a handheld rasping instrument used during surgery to smooth, shape, or prepare bone surfaces or cavities, such as when fitting a prosthetic implant. It is classified as an FDA Class 1 device under 21 CFR 888.4540, indicating minimal risk subject only to general controls. Product code HTP falls under the Orthopedic medical specialty.

510(k) Clearances

5 matches
K Number
Device Name
INTERMEDICS ORTHOPEDICS REAMERS
SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP
CONCEPT ARTHROSCOPY RASP
4MM & 5MM FILE
SUN-LITE BLUE SLIT

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