Cleared Traditional

K161724 - Visicoil MR Marker (User Loaded)

K161724 is the FDA 510(k) clearance for Visicoil MR Marker (User Loaded) by Radiomed Corporation. It is a Class 2 Radiology device (product code IYE) cleared through the Traditional 510(k) pathway after a 310-day FDA review.

K161724 · Radiomed Corporation · Radiology device
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Apr 2017
Decision
310d
Days
Class 2
Risk

K161724 is an FDA 510(k) clearance for the Visicoil MR Marker (User Loaded), Visicoil MR Marker (Pre-Loaded). Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Radiomed Corporation (Bartlett, US). The FDA issued a Cleared decision on April 28, 2017 after a review of 310 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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 Radiomed Corporation devices

Submission Details

510(k) Number K161724 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 22, 2016
Decision Date April 28, 2017
Days to Decision 310 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
203d slower than avg
Panel avg: 107d · This submission: 310d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 316
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