Cleared Traditional

K140013 - SOPIX INSIDE

K140013 is an FDA 510(k) clearance for SOPIX INSIDE, manufactured by Sopro - Acteon Group. The device is a Class 2 Radiology device with product code MUH cleared through the Traditional 510(k) pathway after a 246-day FDA review.

K140013 · Sopro - Acteon Group · Radiology device
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Sep 2014
Decision
246d
Days
Class 2
Risk

K140013 is an FDA 510(k) clearance for the SOPIX INSIDE, SOPIX2 INSIDE. Classified as System, X-ray, Extraoral Source, Digital (product code MUH), Class II - Special Controls.

Submitted by Sopro - Acteon Group (Mt Laurel, US). The FDA issued a Cleared decision on September 5, 2014 after a review of 246 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Sopro - Acteon Group devices

FDA 510(k) Submission Details - K140013

510(k) Number K140013 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 02, 2014
Decision Date September 05, 2014
Days to Decision 246 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
139d slower than avg
Panel avg: 107d · This submission: 246d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MUH Device Classification - Class 2, Special Controls

Product Code MUH System, X-ray, Extraoral Source, Digital
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1800
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 - MUH System, X-ray, Extraoral Source, Digital

All 96
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