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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: OSH FDA class 2

Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis

Orthopedic

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The Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis (product code OSH) is an orthopedic implant system intended to stabilize the thoracolumbar spine as an adjunct to fusion using allograft and/or autograft for the treatment of adolescent idiopathic scoliosis. The system uses pedicle screws and connecting rods to correct and maintain spinal alignment during the fusion process. As an FDA Class 2 device under regulation 888.3070, it requires 510(k) premarket clearance and falls within the Orthopedic specialty. The device is flagged as an implant and is not life-sustaining.

510(k) Clearances

19 matches
K Number
Device Name
OLYMPIC Posterior Spinal Fixation System
CD HORIZON SPINAL SYSTEM
PASS LP SPINAL SYSTEM
IMPLANET SPINE SYSTEM
PASS LP SPINAL SYSTEM
EXPEDIUM, VIPER. VIPER 2 SPINE SYSTEM
POLARIS SPINAL SYSTEM
RANGE SPINAL SYSTEM
CD HORIZON SPINAL SYSTEM
CREO STABILIZATION SYSTEM
RANGE SPINAL SYSTEM
RANGE SPINAL SYSTEM, SMALL STATURE
RESPONSE SPINE SYSTEM
RANGE SPINAL SYSTEM
RANGE SPINAL SYSTEM, SMALL STRATURE COMPONENTS
PASS LP SPINAL SYSTEM
RANGE SPINAL SYSTEM
OP SPINE SYSTEM
OP SPINE 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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