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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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211 records meeting your search criteria returned- Product Code: NRA Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXFORD UNICOMPARTMENTAL KNEE PHASE 3 FEM 03/16/2017
BIOMET UK LTD. OXFORD PARTIAL KNEE SYSTEM DOMED ARCOM L 03/16/2017
BIOMET UK LTD. OXFORD ANATOMIC ARCOM MENISCAL BEARING 03/03/2017
BIOMET UK LTD. OXFORD UNICOMPARTMENTAL KNEE MENISCAL BE 02/24/2017
BIOMET UK LTD. OXFORD UNICOMPARTMENTAL KNEE PHASE 3 RIG 02/23/2017
BIOMET UK LTD. OXFORD UNICOMPARTMENTAL KNEE PHASE 3 FEM 02/23/2017
BIOMET UK LTD. OXFORD UNICOMPARTMENTAL KNEE TIBIAL TRAY 02/23/2017
BIOMET UK LTD. OXFORD UNICOMPARTMENTAL KNEE FEMORAL COM 02/23/2017
BIOMET UK LTD. OXF UNI TIB TRAY SZA LM/RL PMA 01/19/2017
BIOMET UK LTD. OXFORD TIBIAL TRAY SIZE AA LM 12/29/2016
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