Cleared Special

K021990 - GALT MEDICAL GUIDEWIRE

K021990 is an FDA 510(k) clearance for GALT MEDICAL GUIDEWIRE, manufactured by Galt Medical Corp.. The device is a Class 2 Cardiovascular device with product code DQX cleared through the Special 510(k) pathway after a 30-day FDA review.

K021990 · Galt Medical Corp. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2002
Decision
30d
Days
Class 2
Risk

K021990 is an FDA 510(k) clearance for the GALT MEDICAL GUIDEWIRE. Classified as Wire, Guide, Catheter (product code DQX), Class II - Special Controls.

Submitted by Galt Medical Corp. (Garland, US). The FDA issued a Cleared decision on July 18, 2002 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 Galt Medical Corp. devices

FDA 510(k) Submission Details - K021990

510(k) Number K021990 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 18, 2002
Decision Date July 18, 2002
Days to Decision 30 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 125d · This submission: 30d
Pathway characteristics
Modification to existing cleared device.

DQX Device Classification - Class 2, Special Controls

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 682
Devices cleared under the same product code (DQX) and FDA review panel - the closest regulatory comparables to K021990.
HI-TORQUE WHISPER LS
K023300 · Guidant Corp. · Oct 2002
TRANSEND 300 ES GUIDEWIRE, MODEL 46-814 & TRANSEND 300 FLOPPY GUIDEWIRE, MODEL 46-815
K022357 · Boston Scientific, Target · Oct 2002
ILT ADVANCING MECHANISM, MODEL A115AMI
K021638 · Intra Luminal Therapeutics, Inc. · Jul 2002
ILT TORQUER, MODEL 114TR1
K021243 · Intra Luminal Therapeutics, Inc. · Jul 2002
SCOUT (SINUS CORNARIUS UTILITY TOOL), MODEL 335 117
K020821 · Biotronik, Inc. · Jun 2002
MODIFICATION TO SAFE-STEER GUIDE WIRE SYSTEM
K021323 · Intra Luminal Therapeutics, Inc. · May 2002