Sulzer Intratherapeutics, Inc.
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
SKU K023243UPC FGE
In Stock
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IIFDA 510(k) Cleared (K023243)
1
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Sulzer Intratherapeutics, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY is an FDA 510(k)-cleared medical device (K023243) manufactured by Sulzer Intratherapeutics, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 12, 2002. Regulation: 8.
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