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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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11 records meeting your search criteria returned- Product Code: MBB Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
BIOMET FRANCE S.A.R.L. OPTIPAC 40 REFOBACIN BONE CEMENT R-3 03/10/2022
BIOMET FRANCE S.A.R.L. OPTIPAC 40 REFOBACIN BONE CEMENT R-3 03/10/2022
BIOMET FRANCE S.A.R.L. OPTIPAC REFOBACIN PLUS BONE CEMENT 04/27/2018
BIOMET FRANCE S.A.R.L. REFOBACIN PLUS BONE CEMENT 40 04/06/2018
BIOMET FRANCE S.A.R.L. OPTIPAC 01/19/2018
ZIMMER BIOMET, INC. UNKNOWN PALACOS CEMENT 11/03/2017
ZIMMER, INC. COBALT G-HV BONE CEMENT 40G 03/03/2017
BIOMET FRANCE S.A.R.L. UNKNOWN REFOBACIN BONE CEMENT 02/16/2017
BIOMET FRANCE S.A.R.L. UNKNOWN BIOMET REFOBACIN BONE CEMENT 02/16/2017
BIOMET FRANCE S.A.R.L. UNKNOWN REFOBACIN BONE CEMENT 02/16/2017
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