Cleared Special

K051343 - MINI GHOST PTA CATHETER

K051343 is the FDA 510(k) clearance for MINI GHOST PTA CATHETER by NuMED, Inc.. It is a Class 2 Cardiovascular device (product code DQY) cleared through the Special 510(k) pathway after a 66-day FDA review.

K051343 · NuMED, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2005
Decision
66d
Days
Class 2
Risk

K051343 is an FDA 510(k) clearance for the MINI GHOST PTA CATHETER, MODEL 507. Classified as Catheter, Percutaneous (product code DQY), Class II - Special Controls.

Submitted by NuMED, Inc. (Hopkinton, US). The FDA issued a Cleared decision on July 28, 2005 after a review of 66 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1250 - 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 NuMED, Inc. devices

Submission Details

510(k) Number K051343 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 23, 2005
Decision Date July 28, 2005
Days to Decision 66 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
59d faster than avg
Panel avg: 125d · This submission: 66d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code DQY Catheter, Percutaneous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1250
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 - DQY Catheter, Percutaneous

All 577
Devices cleared under the same product code (DQY) and FDA review panel - the closest regulatory comparables to K051343.
ATB ADVANCE PTA DILATATION CATHETER
K052036 · Cook, Inc. · Aug 2005
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K052236 · Bard Peripheral Vascular, Inc. · Aug 2005
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K051846 · Medtronic Vascular · Aug 2005
TRACKER EXCEL -14 PRE-SHAPED MICROCATHETER
K050599 · Boston Scientific Corp · Jun 2005
ANGIODYNAMICS PROFILER PTA BALLOON CATHETER
K051060 · AngioDynamics, Inc. · May 2005
ULTRA-SOFT SV BALLOON DILATATION CATHETER
K050389 · Boston Scientific Corp · May 2005