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: JDR FDA class 2

Staple, Fixation, Bone

Orthopedic

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The Bone Fixation Staple is an orthopedic implant used to stabilize fractures, osteotomies, or bony fusions by spanning a fracture line or joint and holding bone segments in close apposition. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket notification and compliance with general and special controls. The product code is JDR, regulated under 21 CFR 888.3030, within the Orthopedic medical specialty. This device carries the implant flag, indicating it is surgically placed and remains within the body.

510(k) Clearances

50+ matches
K Number
Device Name
Linkt Compression Staple System
Medline UNITE® REFLEX® Hybrid Nitinol Implant System
Arthrex DynaNite Nitinol Staples
TMC Compression Implant System
TMC Compression Implant System
COGNiTiON™ Staple System
A’TOMIC™ Nitinol Fixation System
arcad® 2.0 Duo & Quadro osteosynthesis compressive staples
Medline UNITE® REFLEX® Nitinol Staple Kit
StealthFix Intraosseous Fixation System
Treace Medical Concepts (TMC) Compression Implant System
NITINEX Memory Compression Staple
Medline UNITE® REFLEX® Nitinol Staple System
Extremity Staple
JAWS Nitinol Staple System
JAWS Nitinol Staple System
Treace Medical Concepts (TMC) Implant Fixation System
Tyber Medical Staple Fixation System (various)
DynaClip® Bone Staple
EasyClip® and EasyClip® Xpress
StealthFix Intraosseous Fixation System
FuseForce™ Flex Dynamic Compression System
Medline UNITE REFLEX Nitinol Staple System
Ligament Staple
Arthrex DynaNite Nitinol Staples
DynaClip Bone Staple
Superelastic Staple
DePuy Synthes Hammertoe Continuous Compression Implant
TriMAX Implant System
APTUS Foot System
TriMed Nitinol Staple System
VERTEX Nitinol Staple System
Geo Staple System
DynaClipTM Bone Staple
DynaBridge
MotoCLIP/HiMAX Step Staple Implant System
DePuy Synthes Static Staples
MotoCLIP/HiMAX Implant System
Clench Compression Staple
Orbitum Bone Staple Implant, X and VI
ExoToe Staple
Arthrex DynaNite Nitinol Staple
SNIPER STAPLE SYSTEM, NON-STERILE
Compressyn™ Staple
JAWS(TM) Nitinol Staple System
EPIC Extremely Small Staple
Sniper Staple System
EasyClip Xpress
Memodyn Staple
Stealth Staple System

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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