Cleared Traditional

K092230 - MONA - ORTHOPEDIC MRI SYSTEM

K092230 is an FDA 510(k) clearance for MONA - ORTHOPEDIC MRI SYSTEM, manufactured by Time Medical Limited. The device is a Class 2 Radiology device with product code LNH cleared through the Traditional 510(k) pathway after a 125-day FDA review.

K092230 · Time Medical Limited · Radiology device
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Nov 2009
Decision
125d
Days
Class 2
Risk

K092230 is an FDA 510(k) clearance for the MONA - ORTHOPEDIC MRI SYSTEM, MODEL TMS-200ORTH-01. Classified as System, Nuclear Magnetic Resonance Imaging (product code LNH), Class II - Special Controls.

Submitted by Time Medical Limited (Shanghai, CN). The FDA issued a Cleared decision on November 25, 2009 after a review of 125 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1000 - 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 Time Medical Limited devices

FDA 510(k) Submission Details - K092230

510(k) Number K092230 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 23, 2009
Decision Date November 25, 2009
Days to Decision 125 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
18d slower than avg
Panel avg: 107d · This submission: 125d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

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.

Regulatory Peers - LNH System, Nuclear Magnetic Resonance Imaging

All 842
Devices cleared under the same product code (LNH) and FDA review panel - the closest regulatory comparables to K092230.
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