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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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379 records meeting your search criteria returned- Product Code: KWY Patient Problem: No Information Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN CUP 02/11/2021
ZIMMER BIOMET, INC. UNKNOWN CUP 02/04/2021
ZIMMER BIOMET, INC. UNKNOWN SHELL 01/20/2021
ZIMMER BIOMET, INC. UNKNOWN TAPER 01/11/2021
ZIMMER BIOMET, INC. UNKNOWN STEM 01/11/2021
ZIMMER BIOMET, INC. UNKNOWN CUP 01/11/2021
ZIMMER BIOMET, INC. UNKNOWN LINER 01/07/2021
ZIMMER BIOMET, INC. UNKNOWN LINER 11/30/2020
ZIMMER BIOMET, INC. HIP-VERSYS-UNKNOWN-HEAD 11/30/2020
ZIMMER BIOMET, INC. UNKNOWN G7 CUP 11/19/2020
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