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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 18 Results
ProductCode: FGE Applicant: INTRATHERAPEUTICS, INC. Decision Date To: 06/25/2022
 
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modification to protege self-expanding nitinol stent with starport delivery technology SULZER INTRATHERAPEUTICS, INC. K023243 12/13/2002
modification to protege self-expanding nitinol stent with starport delivery technology SULZER INTRATHERAPEUTICS, INC. K021729 06/21/2002
intrastent ld (large diameter) stent SULZER INTRATHERAPEUTICS, INC. K020528 04/16/2002
modification to protege self-expanding nitinol stent with starport delivery technology SULZER INTRATHERAPEUTICS, INC. K014136 01/17/2002
protege self-expanding nitinol stent with starport delivery technology SULZER INTRATHERAPEUTICS, INC. K011806 09/07/2001
protege self-expanding nitinol stent with starport delivery technology SULZER INTRATHERAPEUTICS, INC. K012347 08/23/2001
intrastent doublestrut paramount xs biliary endoprosthesis INTRATHERAPEUTICS, INC. K011184 08/13/2001
protege self-expanding nitinol stent with starport delivery technology SULZER INTRATHERAPEUTICS, INC. K012066 08/01/2001
intrastent doublestrut paramount xs biliary endoprosthesis INTRATHERAPEUTICS, INC. K003997 01/24/2001
intrastent protege self-expanding nitinol stent with starport delivery technology INTRATHERAPEUTICS, INC. K003040 12/28/2000
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