Cleared Special

K050501 - MODIFICATION TO: XCEED NITINOL SELF-EXP...

K050501 is the FDA 510(k) clearance for MODIFICATION TO: XCEED NITINOL SELF-EXP... by Abbott Vascular Devices. It is a Class 2 Gastroenterology & Urology device (product code FGE) cleared through the Special 510(k) pathway after a 14-day FDA review.

K050501 · Abbott Vascular Devices · Gastroenterology & Urology device
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Mar 2005
Decision
14d
Days
Class 2
Risk

K050501 is an FDA 510(k) clearance for the MODIFICATION TO: XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM. Classified as Stents, Drains And Dilators For The Biliary Ducts (product code FGE), Class II - Special Controls.

Submitted by Abbott Vascular Devices (Redwood, US). The FDA issued a Cleared decision on March 14, 2005 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5010 - the FDA gastroenterology and urology device 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 Abbott Vascular Devices devices

Submission Details

510(k) Number K050501 FDA.gov
FDA Decision Cleared Substantially Equivalent - Abbreviated 510(k) (SESU)
Date Received February 28, 2005
Decision Date March 14, 2005
Days to Decision 14 days
Submission Type Special
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
116d faster than avg
Panel avg: 130d · This submission: 14d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code FGE Stents, Drains And Dilators For The Biliary Ducts
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5010
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FGE Stents, Drains And Dilators For The Biliary Ducts

All 299
Devices cleared under the same product code (FGE) and FDA review panel - the closest regulatory comparables to K050501.
PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907
K050777 · Conmedcorp · Apr 2005
MODIFICATION TO:ZILVER 518 BILIARY STENT
K050698 · Cook, Inc. · Mar 2005
LIFESTENT TURBO BILIARY STENT SYSTEMS
K050627 · Edwards Lifesciences, LLC · Mar 2005
XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM
K050103 · Abbott Laboratories · Feb 2005
MODIFICATION TO: ZILVER 635 BILIARY STENT
K043481 · Cook, Inc. · Dec 2004
LIFESTENT NT35 BILIARY STENT SYSTEM
K042985 · Edwards Lifesciences, LLC · Dec 2004