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: HSN FDA class 2

Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

Orthopedic

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A semi-constrained, cemented, metal/polymer ankle prosthesis is a total ankle replacement implant used to restore joint function in patients with end-stage ankle arthritis, consisting of metallic and polymer components fixed with bone cement. It is classified as an FDA Class 2 device under 21 CFR 888.3110, indicating moderate risk and requiring 510(k) premarket clearance. Product code HSN falls under the Orthopedic medical specialty. This device is an implant.

510(k) Clearances

50+ matches
K Number
Device Name
Incompass Total Ankle System
APEX 3D Total Ankle Replacement System
Hintermann Series H2 Total Ankle System
Prophecy Surgical Planning System
Kinos Total Ankle System
Kinos Total Ankle System
APEX 3D Total Ankle Replacement System
restor3d Kinos Axiom Total Ankle System
QUANTUM® Patient Specific Instrumentation (PSI) System
Kinos Axiom Total Ankle System
Exactech® Vantage® Total Ankle System
Vantage® Total Ankle System
OPTIX H2 Patient Specific Instrument System
QUANTUM Patient Specific Instrumentation (PSI) System
Prophecy Preoperative Navigation Alignment System
MAVEN™ Patient-Specific Instrumentation
QUANTUM® Patient Specific Instrumentation (PSI) System
PROPHECY Preoperative Navigation Alignment System
Apex 3D Total Ankle Replacement System
Maven Patient-Specific Instrumentation
APEX 3D Total Ankle Replacement System
Paragon 28 APEX 3D Total Ankle Replacement System
Kinos Axiom Total Ankle System
Cadence Total Ankle System
The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the INVISION™ Total Ankle Revision System
Quantum® Total Ankle Prosthesis
INFINITY Total Ankle System, INBONE Total Ankle System
Vantage Total Ankle Flat Cut Talar Components
Integra Salto Total Ankle System
INFINITY Total Ankle System
INVISION Total Ankle Revision System
INFINITY Total Ankle System
Hintermann Series H2 Total Ankle System
INVISION Total Ankle Revision System
PROPHECY INVISION Pre-operative Navigation System
PROPHECY INVISION Preoperative Navigation Alignment System
Salto XT, Salto Talaris
INVISION Total Ankle Revision System
Exactech Vantage Total Ankle System
Integra Total Ankle Replacement System
INVISION TOTAL ANKLE REVISION SYSTEM
INFINITY (TM) TOTAL ANKLE SYSTEM; INBONE TOTAL ANKLE SYSTEM
INFINITY TOTAL ANKLE SYSTEM
INBONE TOTAL ANKLE
PROPHECY INFINITY PREOPERATIVE NAVIGATION ALIGNMENT GUIDES
SALTO TALARIS TOTAL ANKLE PROSTHESIS, RHS
INFINITY TOTAL ANKLE SYSTEM
INBONE ( I AND II) TOTAL ANKLE SYSTEMS
DEPUY AGILITY LP TOTAL ANKLE PROSTHESIS
ZIMMER TRABECULAR METAL TOTAL ANKLE

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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