Cleared Traditional

K153026 - Body Pro-Lok Respiratory Plate

K153026 is the FDA 510(k) clearance for Body Pro-Lok Respiratory Plate by Medtec, Inc. D/B/A Civco Medical Solutions. It is a Class 2 Radiology device (product code IYE) cleared through the Traditional 510(k) pathway after a 222-day FDA review.

K153026 · Medtec, Inc. D/B/A Civco Medical Solutions · Radiology device
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Optimized for regulatory review, auditing and printing
May 2016
Decision
222d
Days
Class 2
Risk

K153026 is an FDA 510(k) clearance for the Body Pro-Lok Respiratory Plate, Respiratory Plate Cushion, Body Pro-Respirato.... Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Medtec, Inc. D/B/A Civco Medical Solutions (Orange City, US). The FDA issued a Cleared decision on May 25, 2016 after a review of 222 days - an extended review cycle.

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 Medtec, Inc. D/B/A Civco Medical Solutions devices

Submission Details

510(k) Number K153026 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 16, 2015
Decision Date May 25, 2016
Days to Decision 222 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
115d slower than avg
Panel avg: 107d · This submission: 222d
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

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