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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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9 records meeting your search criteria returned- Product Code: NTE Patient Problem: Reocclusion Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
COVIDIEN SPIDER FX 11/06/2020
INVATEC SPA SPIDER FX 07/09/2020
INVATEC SPA MO.MA 07/09/2020
COVIDIEN SPIDER FX 02/05/2020
COVIDIEN SPIDER FX 11/11/2019
INVATEC SPA MO.MA ULTRA 09/27/2019
INVATEC SPA MO.MA ULTRA 09/17/2019
MEDTRONIC COVIDIEN SPIDER FX 02/13/2018
CORDIS CORPORATION UNKNOWN ANGIOGUARD 02/13/2018
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