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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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123 records meeting your search criteria returned- Product Code: NIP Patient Problem: Insufficient Information Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 03/03/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 03/02/2021
EV3 INC./ MEDTRONIC, INC. PERIPHERAL STENT SYSTEM 03/02/2021
ABBOTT VASCULAR SUPERA 02/26/2021
ABBOTT VASCULAR ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 02/26/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 02/26/2021
W. L. GORE & ASSOCIATES, INC. GORE VIABAHN ENDOPROSTHESIS WITH PROPATE 02/24/2021
W. L. GORE & ASSOCIATES, INC. GORE VIABAHN ENDOPROSTHESIS WITH PROPATE 02/24/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 02/18/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 02/18/2021
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