Cleared Traditional

K813108 - MODEL 500 VERI/500

K813108 is an FDA 510(k) clearance for MODEL 500 VERI/500, manufactured by Verite. The device is a Class 2 Physical Medicine device with product code IPF cleared through the Traditional 510(k) pathway after a 108-day FDA review.

K813108 · Verite · Physical Medicine device
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Feb 1982
Decision
108d
Days
Class 2
Risk

K813108 is an FDA 510(k) clearance for the MODEL 500 VERI/500. Classified as Stimulator, Muscle, Powered (product code IPF), Class II - Special Controls.

Submitted by Verite (Mchenry, US). The FDA issued a Cleared decision on February 19, 1982 after a review of 108 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5850 - the FDA physical medicine device 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 Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

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FDA 510(k) Submission Details - K813108

510(k) Number K813108 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 03, 1981
Decision Date February 19, 1982
Days to Decision 108 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
7d faster than avg
Panel avg: 115d · This submission: 108d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IPF Device Classification - Class 2, Special Controls

Product Code IPF Stimulator, Muscle, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5850
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 Physical Medicine devices follow this clearance model.

Regulatory Peers - IPF Stimulator, Muscle, Powered

All 273
Devices cleared under the same product code (IPF) and FDA review panel - the closest regulatory comparables to K813108.
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RESPOND II...NEUROMUSCULAR STIMULATOR
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