Cleared Traditional

K913803 - INTRALUMINAL ARTERY STRIPPER (FDA 510(k) Clearance)

Class II Cardiovascular device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K913803 · Omni-Tract Surgical, Div. Minn. Scientific, Inc. · Cardiovascular device
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Apr 1992
Decision
242d
Days
Class 2
Risk

K913803 is an FDA 510(k) clearance for the INTRALUMINAL ARTERY STRIPPER. Classified as Stripper, Artery, Intraluminal (product code DWX), Class II - Special Controls.

Submitted by Omni-Tract Surgical, Div. Minn. Scientific, Inc. (St. Paul, US). The FDA issued a Cleared decision on April 24, 1992 after a review of 242 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4875 - the FDA cardiovascular device 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 Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Omni-Tract Surgical, Div. Minn. Scientific, Inc. devices

Submission Details

510(k) Number K913803 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 26, 1991
Decision Date April 24, 1992
Days to Decision 242 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
117d slower than avg
Panel avg: 125d · This submission: 242d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DWX Stripper, Artery, Intraluminal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4875
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 Cardiovascular devices follow this clearance model.