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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 13 Results
ProductCode: KWA Applicant: BIOMET MANUFACTURING CORP Decision Date To: 12/02/2016
 
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porous titanium acetabular augments BIOMET MANUFACTURING CORP. K052888 12/06/2005
altra fx hip system BIOMET MANUFACTURING CORP. K063614 02/20/2007
altra press-fit hip system BIOMET MANUFACTURING CORP. K063002 10/31/2006
compress segmental femoral replacement system (short spindle and anchor plug) BIOMET MANUFACTURING CORP. K062998 01/19/2007
lateralized taperloc microplasty femoral components BIOMET MANUFACTURING CORP. K062994 03/09/2007
m2a magnum 12/14 taper inserts and one-piece modular heads BIOMET MANUFACTURING CORP. K061423 07/27/2006
m2a-magnum tri-spike acetabular component BIOMET MANUFACTURING CORP. K062995 10/31/2006
echo bi-metric press-fit stems BIOMET MANUFACTURING CORP. K070274 04/03/2007
parallel-sided extensively coated femoral stems BIOMET MANUFACTURING CORP. K073637 03/20/2008
arcos interlocking distal stems BIOMET MANUFACTURING CORP. K100469 12/07/2010
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