FDA 510(k) Applications Submitted by AESCULAP IMPLANT SYSTEMS

FDA 510(k) Number Submission Date Device Name Applicant
K140452 02/24/2014 VEGA KNEE SYSTEM AESCULAP IMPLANT SYSTEMS
K121879 06/28/2012 VEGA KNEE SYSTEM AESCULAP IMPLANT SYSTEMS
K090299 02/06/2009 BIOLOX OPTION CERAMIC FEMORAL HEAD AND METHA XL HEADS AESCULAP IMPLANT SYSTEMS
K101815 06/30/2010 ENDURO KNEE SYSTEM AESCULAP IMPLANT SYSTEMS
K071945 07/13/2007 S4 SPINAL SYSTEM AESCULAP IMPLANT SYSTEMS
K100623 03/04/2010 AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM AESCULAP IMPLANT SYSTEMS
K090657 03/12/2009 MODIFICATION TO: S4 SPINAL SYSTEM AESCULAP IMPLANT SYSTEMS


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