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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF ANAT BRG LT LG SIZE 3 PMA 12/14/2015
BIOMET UK LTD. OXF UNI TIB TRAY SZA LM/RL PMA 12/14/2015
BIOMET ORTHOPEDICS OXFORD II TIBIAL PUNCH 12/14/2015
BIOMET UK LTD. OXF UNI C/LESS TIB TRAY LM AA 12/11/2015
BIOMET UK LTD. OXF UNI C/LESS TIB TRAY LM D 12/10/2015
BIOMET UK LTD OXF ANAT BRG LT MD SIZE 3 PMA 12/10/2015
BIOMET UK LTD. OXF ANAT BRG LT MD SIZE 4 PMA 12/10/2015
BIOMET UK LTD. OXF UNI C/LESS TIB TRAY LM D 12/09/2015
BIOMET UK LTD. OXF UNI C/LESS TIB TRAY RM C 12/09/2015
BIOMET UK LTD. OXF UNI TIB TRAY SZ D LM PMA 12/07/2015
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