Cleared Special

K182315 - Magic Torque DLVR Guidewire

K182315 is the FDA 510(k) clearance for Magic Torque DLVR Guidewire by Boston Scientific Corporation. It is a Class 2 Cardiovascular device (product code DQX) cleared through the Special 510(k) pathway after a 30-day FDA review.

K182315 · Boston Scientific Corporation · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2018
Decision
30d
Days
Class 2
Risk

K182315 is an FDA 510(k) clearance for the Magic Torque DLVR Guidewire. Classified as Wire, Guide, Catheter (product code DQX), Class II - Special Controls.

Submitted by Boston Scientific Corporation (Maple Grove, US). The FDA issued a Cleared decision on September 26, 2018 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1330 - the FDA cardiovascular device oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Boston Scientific Corporation devices

Submission Details

510(k) Number K182315 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 27, 2018
Decision Date September 26, 2018
Days to Decision 30 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 125d · This submission: 30d
Pathway characteristics
Modification to existing cleared device.

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 501
Devices cleared under the same product code (DQX) and FDA review panel - the closest regulatory comparables to K182315.
Lunderquist® Fixed Core Wire Guide
K181353 · Cook Incorporated · Feb 2019
Roadrunner Extra Support Wire Guide
K183467 · Cook Incorporated · Jan 2019
Reuter Tip Deflecting Wire Guide
K180830 · Cook Incorporated · Dec 2018
Bandit guidewire
K181647 · Vascular Solutions, Inc. · Jul 2018
ASAHI PTCA Guide Wire ASAHI Gladius Mongo 14, ASAHI Gladius Mongo 14 ES
K180784 · Asahi Intecc Co., Ltd. · Jul 2018
ASAHI PTCA Guide Wire ASAHI SION black
K173277 · Asahi Intecc Co., Ltd. · Jul 2018