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: JDZ FDA class 1

Mixer, Cement, For Clinical Use

Orthopedic

View full classification →

A Cement Mixer for Clinical Use is an orthopedic surgical instrument used to combine the components of polymethylmethacrylate (PMMA) bone cement under controlled conditions, often under vacuum, to reduce porosity and improve the mechanical properties of the resulting cement. It is classified as FDA Class 1 (lowest risk), subject only to general controls including proper labeling and manufacturing standards. The product code is JDZ, regulated under 21 CFR 888.4210, within the Orthopedic medical specialty. No special flags apply to this device.

510(k) Clearances

13 matches
K Number
Device Name
EXACTECH ALL POLY ACETABULAR CUP
PRISM BONE CEMENT MIXING SYSTEM
STRYKER HIGH VACUUM BONE CEMENT MIXER/INJECT SYST
REUSABLE BOWL AND SPATULA FOR MIXING BONE CEMENTS
ZIMMER VACUUM MIXING SYSTEM
MIX EVAC II
SIMPLEX ENHANCEMENT MIXER
CEMENTRIFUGE
ZIMMER BONE CEMENT CENTRIFUGATION SYS
HOWMEDICA MIX-KIT II
MIXING BOWL & SPATULA, DISPOSABLE
ORTHOMIX
MIX EVAC BONE CEMENT

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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