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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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7 records meeting your search criteria returned- Product Code: KWA Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2015
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ManufacturerBrand NameDate Report Received
Unknown Manufacturer BHR ACETABULAR CUP 50MM 07/22/2020
ZIMMER BIOMET, INC. UNKNOWN FEMORAL HEAD 02/24/2020
ZIMMER BIOMET, INC. UNKNOWN FEMORAL STEM 02/24/2020
ZIMMER BIOMET, INC. UNKNOWN STEM 08/29/2019
ZIMMER BIOMET, INC. UNKNOWN HG CUP 08/29/2019
BIOMET UK LTD. RECAP RESURFACING SYSTEM FEMORAL HEAD SZ 11/18/2016
BIOMET UK LTD. RECAP/MAGNUM ACETABULAR SHELL SZ 48X42MM 11/18/2016
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