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: OLO FDA class 2

Orthopedic Stereotaxic Instrument

Neurology

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The Orthopedic Stereotaxic Instrument (product code OLO) is a Class 2 device regulated under 21 CFR 882.4560 in the Neurology specialty (NE), cleared through the 510(k) pathway and reviewed by the Orthopedic panel. It provides stereotaxic guidance during orthopedic surgical procedures including joint or spine surgery, and is distinct from neurological stereotaxic instruments classified under product code HAW. The device is not an implant and is not life-sustaining.

510(k) Clearances

50+ matches
K Number
Device Name
Dynamis Robotic Surgical System
CORUS™ Navigation System-GN
SIMPACT Sacroiliac Joint Fixation System GX Navigation Instruments
Navigated LLIF Impactable Tracker
CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody
Ion-C Navigation Instruments
ROSA® Shoulder System
Pytheas Your Guided Trajectory
Foundation Surgical Navigated Lateral Disc Prep Instruments
SPINEART Navigation Instrument System
SYMPHONY Navigation Ready Instruments
REAL INTELLIGENCE™ CORI™
CUVIS-joint (CJ150)
TiLink-L Navigation Instruments
EUROPA™ Posterior Cervical Fusion Navigated Instruments
Q Pedicle Instruments
TMINI® Miniature Robotic System
Mako Total Knee Application
“POINT” Kinguide Agile Hybrid Navigation System; DRF Accessories Set
Valence Robotic Navigation System; Valence Robotic Navigation Instruments (For Use with StealthStation)
VERTICALE GPS Instruments
Spine Guidance 5.4 Software; Spine Guidance 5.4 Upgrade; Spine Guidance 5.4 Update; Spine Guidance 5.4 Software Enable; Spine Guidance 5.4 Sales Demo; Q Drill Tracker; NavLock Adapter; Elite Q Attacments; Elite Cutting Accessories; Maestro Air Motor
Stealth AXiS™ Surgical System with Stealth AXiS™ Spine clinical application
Spine Guidance 5.3 Software; Q Interbody Instruments; Elite Q Attachments; Elite Cutting Accessories
Q Interbody Instruments
ROSA Knee System with UltraSound Imaging Platform (USIP)
Navigation Module of the Cortium® System
POINT Kinguide Agile Robotic Arm Surgical Stereotactic System
DYNAMIS™ Navigation System
TMINI Miniature Robotic System
Paradigm System
REAL INTELLIGENCE™ CORI™ XT (CORI XT)
Spineology Navigation Instruments
Rosa® Knee System
ExcelsiusGPS™ Instruments
Firebird SI Navigation System
Navigated Instruments
OsteoCentric Navigated Instruments System
StealthStation S8 Spine Software
TMINI Miniature Robotic System
RPS Primary TKA Software; RPS Console; RPS Saw One; RPS Cable; RPS Saw Oscillating Tip Cartridge; RPS Console Cart Attachment; Ball Tip Pointer
iGPS Navigation Instruments
Spine & Trauma Navigation Instruments
Mazor X System / Mazor X Stealth Edition
Evolution Spine Navigation Instruments
CORUS™ Navigation System-GX
Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments)
TMINI Miniature Robotic System
SPINEART Navigation Instrument System
Stealth™ Spine Clamps; ModuLeX™ Shank Mounts

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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