Cleared Special

K081220 - MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER

K081220 is an FDA 510(k) clearance for MODIFICATION TO ANGIOSCULPT PTA SCORING..., manufactured by Angioscore, Inc.. The device is a Class 2 Cardiovascular device with product code PNO cleared through the Special 510(k) pathway after a 28-day FDA review.

K081220 · Angioscore, Inc. · Cardiovascular device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
May 2008
Decision
28d
Days
Class 2
Risk

K081220 is an FDA 510(k) clearance for the MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER. Classified as Catheter, Percutaneous, Cutting/scoring (product code PNO), Class II - Special Controls.

Submitted by Angioscore, Inc. (Fremont, US). The FDA issued a Cleared decision on May 28, 2008 after a review of 28 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.

FDA 510(k) Submission Details - K081220

510(k) Number K081220 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 30, 2008
Decision Date May 28, 2008
Days to Decision 28 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
97d faster than avg
Panel avg: 125d · This submission: 28d
Pathway characteristics
Modification to existing cleared device.

PNO Device Classification - Class 2, Special Controls

Product Code PNO Catheter, Percutaneous, Cutting/scoring
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1250
Definition To Reduce Vascular Stenosis By Dilatation And Apposition Of The Cutting/scoring Surfaces To The Stenotic Material
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 - PNO Catheter, Percutaneous, Cutting/scoring

All 45
Devices cleared under the same product code (PNO) and FDA review panel - the closest regulatory comparables to K081220.
ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076-6040, 2092-6040, 2105-6040
K091966 · Angioscore, Inc. · Jul 2009
VASCUTRAK 2, MODELS: V14 AND V18
K082343 · Ymed, Inc. · Sep 2008
ANGIOSCULPT PTA SCORING BALLOON CATHETER
K082059 · Angioscore, Inc. · Aug 2008
ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076 AND 2039
K080151 · Angioscore, Inc. · Apr 2008
VASCUTRAK II PTA DILATATION CATHETER
K073025 · Thermopeutix, Inc. Dba Ymed, Inc. · Nov 2007
ANGIOSCULPT PTA SCORING BALLOON CATHETER
K072225 · Angioscore, Inc. · Oct 2007
K081220 · MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER
Download PDF FDA Summary Angioscore, Inc.