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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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252 records meeting your search criteria returned- Product Code: NRA Patient Problem: Insufficient Information Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF ANAT BRG LT MD SIZE 4 PMA 09/28/2022
BIOMET UK LTD. OXF UNI TIB TRAY SZ B LM PMA 09/28/2022
BIOMET UK LTD. UNKNOWN OXFORD TIBIAL COMPONENT 09/12/2022
BIOMET UK LTD. UNKNOWN OXFORD BEARING 09/12/2022
BIOMET UK LTD. UNKNOWN OXFORD FEMORAL COMPONENT 09/12/2022
BIOMET UK LTD. OXFORD PKS CEMENTED TIBIA, ALPHA, STANDA 06/01/2022
BIOMET UK LTD. OXFORD PKS TWIN PEG FEMUR - SMALL 06/01/2022
BIOMET UK LTD. OXFORD PKS ANATOMIC ARCOM MENISCAL BRG - 06/01/2022
BIOMET UK LTD. OXF ANAT BRG RT SM SIZE 3 PMA 05/11/2022
BIOMET UK LTD. OXF ANAT BRG LT MD SIZE 3 PMA 04/29/2022
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