Cleared Special

K062417 - XPLORER 1100

K062417 is an FDA 510(k) clearance for XPLORER 1100, manufactured by Imaging Dynamics Company , Ltd.. The device is a Class 2 Radiology device with product code KPR cleared through the Special 510(k) pathway after a 28-day FDA review.

K062417 · Imaging Dynamics Company , Ltd. · Radiology device
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Sep 2006
Decision
28d
Days
Class 2
Risk

K062417 is an FDA 510(k) clearance for the XPLORER 1100. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Imaging Dynamics Company , Ltd. (Calgary, Alberta, CA). The FDA issued a Cleared decision on September 15, 2006 after a review of 28 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 Imaging Dynamics Company , Ltd. devices

FDA 510(k) Submission Details - K062417

510(k) Number K062417 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 18, 2006
Decision Date September 15, 2006
Days to Decision 28 days
Submission Type Special
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 107d · This submission: 28d
Pathway characteristics
Modification to existing cleared device.

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 264
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K062417.
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ORTHOXP
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K062405 · Imaging Dynamics Company , Ltd. · Sep 2006
XAMINER
K061595 · Imaging Dynamics Company , Ltd. · Aug 2006