Cleared Traditional

K140351 - ARROW GPSCATH BALLOON DILATATION CATHETER

K140351 is an FDA 510(k) clearance for ARROW GPSCATH BALLOON DILATATION CATHETER, manufactured by Hotspur Technologies,Inc Subsidiary of Teleflex ME. The device is a Class 2 Cardiovascular device with product code LIT cleared through the Traditional 510(k) pathway after a 141-day FDA review.

K140351 · Hotspur Technologies,Inc Subsidiary of Teleflex ME · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2014
Decision
141d
Days
Class 2
Risk

K140351 is an FDA 510(k) clearance for the ARROW GPSCATH BALLOON DILATATION CATHETER. Classified as Catheter, Angioplasty, Peripheral, Transluminal (product code LIT), Class II - Special Controls.

Submitted by Hotspur Technologies,Inc Subsidiary of Teleflex ME (Mountain View, US). The FDA issued a Cleared decision on July 2, 2014 after a review of 141 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1250 - 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 Hotspur Technologies,Inc Subsidiary of Teleflex ME devices

FDA 510(k) Submission Details - K140351

510(k) Number K140351 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 11, 2014
Decision Date July 02, 2014
Days to Decision 141 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
16d slower than avg
Panel avg: 125d · This submission: 141d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LIT Device Classification - Class 2, Special Controls

Product Code LIT Catheter, Angioplasty, Peripheral, Transluminal
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 - LIT Catheter, Angioplasty, Peripheral, Transluminal

All 278
Devices cleared under the same product code (LIT) and FDA review panel - the closest regulatory comparables to K140351.
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K132020 · Cook, Inc. · Oct 2013
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