FDA 510(k) Applications Submitted by SUSAN ALEXANDER

FDA 510(k) Number Submission Date Device Name Applicant
K070274 01/29/2007 ECHO BI-METRIC PRESS-FIT STEMS BIOMET MANUFACTURING CORP.
K060303 02/06/2006 VANGUARD PS OPEN BOX POROUS FEMORAL COMPONENTS BIOMET MANUFACTURING CORP.
K070389 02/09/2007 PEEK KNOTLESS ANCHORS BIOMET SPORTS MEDICINE, INC.
K080361 02/11/2008 REGENEREX TIBIAL COMPONENTS BIOMET, INC.
K060692 03/15/2006 COMPREHENSIVE PRIMARY SHOULDER STEMS BIOMET MANUFACTURING CORP.
K060716 03/17/2006 VERSA-DIAL HUMERAL HEAD PROSTHESIS BIOMET MANUFACTURING CORP.
K070823 03/26/2007 GROWTH CONTROL PLATING SYSTEM BIOMET TRAUMA
K081243 05/01/2008 BIOMET PHOENIX ANKLE NAIL SYSTEM BIOMET TRAUMA
K071325 05/10/2007 BIOMET VARIABLE LOCKING PLATE SYSTEM BIOMET TRAUMA
K091608 06/03/2009 COBALT MV BONE CEMENT BIOMET MANUFACTURING CORP.
K061801 06/26/2006 2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS ARTHROTEK, INC.
K092150 07/16/2009 COBALT MV WITH GENTAMICIN (AKA COBALT G-MV) BONE CEMENT BIOMET, INC.
K042552 09/20/2004 BIO-CORE INTERFERENCE SCREW BIOMET, INC.
K082826 09/25/2008 VANGUARD CR STEM HOUSINGS BIOMET MANUFACTURING CORP.
K052639 09/26/2005 GENERATION 4 POLISHED FEMORAL HIP PROSTHESIS WITH PROXIMAL CEMENT SPACER BIOMET MANUFACTURING, INC.
K072879 10/09/2007 INNERVUE DIAGNOSTIC SCOPE SYSTEM BIOMET ORTHOPEDICS, INC.
K063393 11/09/2006 SMALL STATURE SPACERS BIOMET SPINE
K063515 11/21/2006 TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II UNICONDYLAR KNEE BIOMET MANUFACTURING, INC.
K053461 12/13/2005 EZLOC FEMORAL FIXATION DEVICE ARTHROTEK, INC.
K083782 12/19/2008 REGENEREX PATELLA COMPONENTS BIOMET MANUFACTURING CORP.


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