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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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430 records meeting your search criteria returned- Product Code: NRA Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF ANAT BRG RT SM SIZE 4 PMA 12/17/2020
BIOMET UK LTD. OXFORD UNI TWIN-PEG FEMORAL SM 12/07/2020
BIOMET UK LTD. OXF ANAT BRG LT SM SIZE 3 PMA 12/07/2020
BIOMET UK LTD. OXF UNI TIB TRAY SZA LM 12/07/2020
BIOMET UK LTD. OXF ANAT BRG LT LG SIZE 3 PMA 11/18/2020
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 6 PMA 09/04/2020
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 4 PMA 08/07/2020
BIOMET UK LTD. OXF ANAT BRG LT SM SIZE 9 PMA 08/04/2020
BIOMET UK LTD. OXF ANAT BRG LT LG SIZE 5 PMA 07/20/2020
BIOMET UK LTD. OXF ANAT BRG LT SM SIZE 6 PMA 06/11/2020
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