Cleared Traditional

K152994 - Adaptivo

K152994 is an FDA 510(k) clearance for Adaptivo, manufactured by Aurora Technology Development, LLC. The device is a Class 2 Radiology device with product code IYE cleared through the Traditional 510(k) pathway after a 113-day FDA review.

K152994 · Aurora Technology Development, LLC · Radiology device
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Feb 2016
Decision
113d
Days
Class 2
Risk

K152994 is an FDA 510(k) clearance for the Adaptivo. Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Aurora Technology Development, LLC (Madison, US). The FDA issued a Cleared decision on February 3, 2016 after a review of 113 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 Aurora Technology Development, LLC devices

FDA 510(k) Submission Details - K152994

510(k) Number K152994 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 13, 2015
Decision Date February 03, 2016
Days to Decision 113 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
6d slower than avg
Panel avg: 107d · This submission: 113d
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

All 367
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