Cleared Traditional

K200756 - Kubtec Mozart Supra (FDA 510(k) Clearance)

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K200756 · Kub Technologies, Inc. · Radiology device
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Jun 2020
Decision
80d
Days
Class 2
Risk

K200756 is an FDA 510(k) clearance for the Kubtec Mozart Supra. Classified as Cabinet, X-ray System (product code MWP), Class II - Special Controls.

Submitted by Kub Technologies, Inc. (Stratford, US). The FDA issued a Cleared decision on June 12, 2020 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Kub Technologies, Inc. devices

Submission Details

510(k) Number K200756 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 24, 2020
Decision Date June 12, 2020
Days to Decision 80 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 107d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MWP Cabinet, X-ray System
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1680
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - MWP Cabinet, X-ray System

All 26
Devices cleared under the same product code (MWP) and FDA review panel - the closest regulatory comparables to K200756.
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Solas OR
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K210956 · Kub Technologies, Inc. · Aug 2021
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K210957 · Kub Technologies, Inc. · Aug 2021