Cleared Traditional

K070664 - PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).

K070664 is an FDA 510(k) clearance for PROGENY IMAGING SOFTWARE, manufactured by Progeny, Inc.. The device is a Class 2 Radiology device with product code MUH cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K070664 · Progeny, Inc. · Radiology device
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Optimized for regulatory review, auditing and printing
Apr 2007
Decision
48d
Days
Class 2
Risk

K070664 is an FDA 510(k) clearance for the PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).. Classified as System, X-ray, Extraoral Source, Digital (product code MUH), Class II - Special Controls.

Submitted by Progeny, Inc. (Buffalo Grove, US). The FDA issued a Cleared decision on April 26, 2007 after a review of 48 days - a notably fast clearance 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: 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 Progeny, Inc. devices

FDA 510(k) Submission Details - K070664

510(k) Number K070664 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 09, 2007
Decision Date April 26, 2007
Days to Decision 48 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
59d faster than avg
Panel avg: 107d · This submission: 48d
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

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