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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 UNI FEMORAL MD 05/05/2017
BIOMET UK LTD. OXFORD UNICOMPARTMENTAL KNEE PHASE 3 FEM 05/05/2017
BIOMET UK LTD. OXFORD PKS COCR SIZE B LM STD 05/05/2017
BIOMET UK LTD. UNKNOWN KNEE 05/05/2017
BIOMET UK LTD. OXFORD PARTIAL KNEE SYSTEM RIGHT MEDIAL 04/17/2017
BIOMET UK LTD. OXFORD ANATOMICAL BEARING SZ 6 04/07/2017
BIOMET UK LTD. OXFORD PKS COCR SIZE C LM STD 04/05/2017
BIOMET UK LTD. OXFORD PARTIAL KNEE SYSTEM SIZE C LEFT M 03/31/2017
BIOMET UK LTD. OXFORD PARTIAL KNEE SYSTEM CEMENTED TWIN 03/31/2017
BIOMET UK LTD. UNKNOWN OXFORD 03/30/2017
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