Cleared Traditional

K983267 - DIGORA FOR WINDOWS 2.0

K983267 is an FDA 510(k) clearance for DIGORA FOR WINDOWS 2.0, manufactured by Orion Corporation Soredex. The device is a Class 2 Radiology device with product code MUH cleared through the Traditional 510(k) pathway after a 104-day FDA review.

K983267 · Orion Corporation Soredex · Radiology device
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Dec 1998
Decision
104d
Days
Class 2
Risk

K983267 is an FDA 510(k) clearance for the DIGORA FOR WINDOWS 2.0. Classified as System, X-ray, Extraoral Source, Digital (product code MUH), Class II - Special Controls.

Submitted by Orion Corporation Soredex (Helsinki, FI). The FDA issued a Cleared decision on December 30, 1998 after a review of 104 days - within the typical 510(k) review window.

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 Orion Corporation Soredex devices

FDA 510(k) Submission Details - K983267

510(k) Number K983267 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 17, 1998
Decision Date December 30, 1998
Days to Decision 104 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
3d faster than avg
Panel avg: 107d · This submission: 104d
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.