Cleared Traditional

K011111 - MXD100/MX 20, OR MX 30, OR MX 40 OR MX 50--(MXD 100 SERIES)

K011111 is an FDA 510(k) clearance for MXD100/MX 20, manufactured by Modular X-Ray Devices. The device is a Class 2 Radiology device with product code KPR cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K011111 · Modular X-Ray Devices · Radiology device
Download Printable Device Report (PDF)
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May 2001
Decision
49d
Days
Class 2
Risk

K011111 is an FDA 510(k) clearance for the MXD100/MX 20, OR MX 30, OR MX 40 OR MX 50--(MXD 100 SERIES). Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Modular X-Ray Devices (Roodepoort, ZA). The FDA issued a Cleared decision on May 30, 2001 after a review of 49 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 Modular X-Ray Devices devices

FDA 510(k) Submission Details - K011111

510(k) Number K011111 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 11, 2001
Decision Date May 30, 2001
Days to Decision 49 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
58d faster than avg
Panel avg: 107d · This submission: 49d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KPR Device Classification - Class 2, Special Controls

Product Code KPR System, X-ray, Stationary
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 - KPR System, X-ray, Stationary

All 263
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K011111.
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