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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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17 records meeting your search criteria returned- Product Code: NRA Patient Problem: No Patient Involvement Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXFORD PH3 CEMENTLESS FEM SZ S 09/07/2020
BIOMET UK LTD. OXFORD UNI TWIN-PEG FEMORAL SM 02/03/2020
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 3 PMA 01/15/2020
BIOMET UK LTD. OXFORD UNI TWIN-PEG FEMORAL SM 12/13/2019
BIOMET UK LTD. OXF CMNTLS IMPLANT INSERT IMPACTOR 11/01/2019
BIOMET UK LTD. TINBN VG INT PS ANAT FM L 70MM 70 MM 10/02/2019
BIOMET UK LTD. OXF TWIN-PEG CMNTD FEM XL PMA 09/09/2019
BIOMET UK LTD. OXF UNI TIB TRAY SZ D RM PMA 02/19/2019
BIOMET UK LTD. OXF UNI TIB TRAY SZ D LM PMA 01/02/2019
BIOMET UK LTD. OXF UNI CMNTLS TIB SZ D LM 12/05/2018
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