Cleared Traditional

K875323 - MODIFIED SCHNEIDER-SHILEY WIRE TORQUER

K875323 is the FDA 510(k) clearance for MODIFIED SCHNEIDER-SHILEY WIRE TORQUER by Schneider-Shilley (Usa). It is a Class 2 Cardiovascular device (product code DQX) cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K875323 · Schneider-Shilley (Usa) · Cardiovascular device
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Mar 1988
Decision
90d
Days
Class 2
Risk

K875323 is an FDA 510(k) clearance for the MODIFIED SCHNEIDER-SHILEY WIRE TORQUER. Classified as Wire, Guide, Catheter (product code DQX), Class II - Special Controls.

Submitted by Schneider-Shilley (Usa) (Minneapolis, US). The FDA issued a Cleared decision on March 28, 1988 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1330 - 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 Schneider-Shilley (Usa) devices

Submission Details

510(k) Number K875323 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 29, 1987
Decision Date March 28, 1988
Days to Decision 90 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
35d faster than avg
Panel avg: 125d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DQX Wire, Guide, Catheter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1330
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.

Regulatory Peers - DQX Wire, Guide, Catheter

All 502
Devices cleared under the same product code (DQX) and FDA review panel - the closest regulatory comparables to K875323.
ACS HI-TORQUE STANDARD & INTERMEDI. GUIDE WIRE
K881787 · Advanced Cardiovascular Systems, Inc. · Jul 1988
ACS HI-TORQUE GUIDE WIRES
K874202 · Advanced Cardiovascular Systems, Inc. · Apr 1988
GUIDE WIRE INTRODUCER
K873972 · Target Therapeutics · Apr 1988
CORDIS STEERABLE GUIDEWIRE
K873403 · Cordis Corp. · Mar 1988
ACS 0.025-IN HI-TORQ MODIF J/STAND TELESC GUIDEWIR
K874776 · Advanced Cardiovascular Systems, Inc. · Feb 1988
TELEFLEX STEERABLE GUIDEWIRE
K871850 · Teleflexmedical, Inc. · Jan 1988