Cleared Traditional

K162265 - CushionCast Moldable Cushions

K162265 is an FDA 510(k) clearance for CushionCast Moldable Cushions, manufactured by Izi Medical Products, LLC. The device is a Class 2 Radiology device with product code IYE cleared through the Traditional 510(k) pathway after a 96-day FDA review.

K162265 · Izi Medical Products, LLC · Radiology device
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Nov 2016
Decision
96d
Days
Class 2
Risk

K162265 is an FDA 510(k) clearance for the CushionCast Moldable Cushions. Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Izi Medical Products, LLC (Owings Mills, US). The FDA issued a Cleared decision on November 15, 2016 after a review of 96 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5050 - 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 Izi Medical Products, LLC devices

FDA 510(k) Submission Details - K162265

510(k) Number K162265 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 11, 2016
Decision Date November 15, 2016
Days to Decision 96 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
11d faster than avg
Panel avg: 107d · This submission: 96d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYE Device Classification - Class 2, Special Controls

Product Code IYE Accelerator, Linear, Medical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5050
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 - IYE Accelerator, Linear, Medical

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