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: KWD FDA class 2

Prosthesis, Toe, Hemi-, Phalangeal

Orthopedic

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The Phalangeal Hemi Toe Prosthesis is an orthopedic implant designed to replace one articular surface of a toe joint, used to treat conditions such as arthritis or deformity of the toes while preserving some natural joint structure. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification before marketing. The product code is KWD, regulated under 21 CFR 888.3730, in the Orthopedic medical specialty. This device is an implant.

510(k) Clearances

45 matches
K Number
Device Name
Accu-Joint Hemi Implant
Montross Extremity Medical Hemi Implant System
BioPoly Lesser Toe Hemiarthroplasty Implant
restor3d MTP Implant
BioPoly Great Toe Hemiarthroplasty Implant
Accu-Joint Hemi Implant
BOSS Toe Fixation System
Cannulated Hemi Implant
Life Spine Metatarsal Hemi Implant
HemiCAP MTP Resurfacing Hemi-Arthroplasty System
HEMICAP MTP RESURFACING HEMI-ARTHROPLASTY IMPLANT
LESSER METATARSAL HEAD IMPLANT SYSTEM
BIOPRO HEMI-EDGE TOE SYSTEM
METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET
HEMI PHALANGEAL IMPLANT SURGICAL INSTRUMENT SET
HEMI IMPLANT; MINI HEMI IMPLANT
ASCENSION METAL GREAT TOE SYSTEM
METATARSAL DECOMPRESSION IMPLANT, MODEL 100
METASURG CANNULATED TIATANIUM HEMI IMPLANT, MODEL HM-1000
OSTEOMED RESURFACING METATARSAL IMPLANT WITH HYDROXYLAPATITE COATING
SBI SR MTP TOE IMPLANT
OSTEOMED METATARSAL RESURFACING IMPLANT SYSTEM
3S HEMI TOE
METAL HEMI IMPLANT
MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION
CAP 7.0MM MTP RESURFACING HEMI-ARTHROPLASTY
ARTHREX ANATOEMIC PHALANGEAL PROSTHESIS
ORTHROPRO HEMI TOE
SBI TRIHEDRON MTP HEMI GT
OSTEOMED 1ST MPJ HEMI IMPLANT SYSTEM
ASCENSION PYROSPHERE CMC/TMT
TOE MP JOINT, MODELS 10412-10414, 14958, 14960, 1060-10062,16818,-16822,16867-16870
CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365
CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT
ORTHOSPHERE CERAMIC SPHERICAL IMPLANT
K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)
GREAT TOE IMPLANT
GREAT TOE IMPLANT SYSTEM
MTP RESESURFACING JOINT-SMALL/9301-01; MEDIUM/9301-02; LARGE/9301-03
FUTURA BIOMEDICAL METAL HEMI TOE IMPLANT
TOWNLEY GREAT TOE JOINT
SUTTER PHALANGEAL CAP
SWANSON TITANIUM GREAT TOE IMPLANT
SUTTER LESSER METATARSAL CAP
IMPLANT, H.P. CONDYLAR

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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