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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
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4 records meeting your search criteria returned- Product Code: KWS Patient Problem: Atrial Fibrillation Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US CROSSLINK ANCHOR PG GLENOID 52 08/26/2019
DEPUY IRELAND - 9616671 HUMERAL HEAD SIZE 54 08/26/2019
DEPUY IRELAND - 9616671 ANCHOR PLATE SIZE 54 08/26/2019
ZIMMER BIOMET, INC. UNKNOWN HUMERAL STEM 02/23/2018
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