
Vascular Architects, Inc.
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VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTROLLED EXPANSION DELIVERY SYSTEM is an FDA 510(k)-cleared medical device (K012544) manufactured by Vascular Architects, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 14, 2001. Regulation: 8.