Cleared Special

K050237 - STARSHIELD V3 RF TRNT

K050237 is an FDA 510(k) clearance for STARSHIELD V3 RF TRNT, manufactured by Odin Medical Technologies , Ltd.. The device is a Class 2 Radiology device with product code LNH cleared through the Special 510(k) pathway after a 44-day FDA review.

K050237 · Odin Medical Technologies , Ltd. · Radiology device
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Mar 2005
Decision
44d
Days
Class 2
Risk

K050237 is an FDA 510(k) clearance for the STARSHIELD V3 RF TRNT. Classified as System, Nuclear Magnetic Resonance Imaging (product code LNH), Class II - Special Controls.

Submitted by Odin Medical Technologies , Ltd. (Yokneam Elit, IL). The FDA issued a Cleared decision on March 18, 2005 after a review of 44 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 Odin Medical Technologies , Ltd. devices

FDA 510(k) Submission Details - K050237

510(k) Number K050237 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 02, 2005
Decision Date March 18, 2005
Days to Decision 44 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
63d faster than avg
Panel avg: 107d · This submission: 44d
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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