Aspire Covered Stent and Delivery Catheter

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K003173 ↗

FDA Product Code

ESW

Device Class

Class II

Regulation

21 CFR Part 878.3610

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Vascular Architects Aspire Covered Stent and Controlled Expansion Delivery System

  Class II

  FDA 510(k) K012544 Active Cleared 15 Nov 2001

• Modification to Vascular Architects Aspire Covered Stent and Contrilled Expansion Delivery System

  Class II

  FDA 510(k) K030567 Active Cleared 24 Mar 2003

• Vascular Architects Periscope Device

  Class II

  FDA 510(k) K003719 Active Cleared 28 Feb 2001

• Aspire Covered Stent and 718 Delivery System

  Class II

  FDA 510(k) K031641 Active Cleared 1 Aug 2003