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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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