Cleared Special

K080048 - MSK EXTREME MR SCANNER, MODEL AA5000

K080048 is an FDA 510(k) clearance for MSK EXTREME MR SCANNER, manufactured by Oni Medical Systems, Inc.. The device is a Class 2 Radiology device with product code LNH cleared through the Special 510(k) pathway after a 29-day FDA review.

K080048 · Oni Medical Systems, Inc. · Radiology device
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Feb 2008
Decision
29d
Days
Class 2
Risk

K080048 is an FDA 510(k) clearance for the MSK EXTREME MR SCANNER, MODEL AA5000. Classified as System, Nuclear Magnetic Resonance Imaging (product code LNH), Class II - Special Controls.

Submitted by Oni Medical Systems, Inc. (Wilmington, US). The FDA issued a Cleared decision on February 6, 2008 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1000 - 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 Oni Medical Systems, Inc. devices

FDA 510(k) Submission Details - K080048

510(k) Number K080048 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 08, 2008
Decision Date February 06, 2008
Days to Decision 29 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
78d faster than avg
Panel avg: 107d · This submission: 29d
Pathway characteristics
Modification to existing cleared device.

LNH Device Classification - Class 2, Special Controls

Product Code LNH System, Nuclear Magnetic Resonance Imaging
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1000
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.

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