Cleared Special

K123005 - DDRVERSA MOTION

K123005 is an FDA 510(k) clearance for DDRVERSA MOTION, manufactured by Swissray Medical AG. The device is a Class 2 Radiology device with product code MQB cleared through the Special 510(k) pathway after a 71-day FDA review.

K123005 · Swissray Medical AG · Radiology device
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Dec 2012
Decision
71d
Days
Class 2
Risk

K123005 is an FDA 510(k) clearance for the DDRVERSA MOTION. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Swissray Medical AG (Naples, US). The FDA issued a Cleared decision on December 7, 2012 after a review of 71 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Swissray Medical AG devices

FDA 510(k) Submission Details - K123005

510(k) Number K123005 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 27, 2012
Decision Date December 07, 2012
Days to Decision 71 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
36d faster than avg
Panel avg: 107d · This submission: 71d
Pathway characteristics
Modification to existing cleared device.

MQB Device Classification - Class 2, Special Controls

Product Code MQB Solid State X-ray Imager (flat Panel/digital Imager)
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 - MQB Solid State X-ray Imager (flat Panel/digital Imager)

All 294
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