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Aesculap Implant System, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K142707AIS Odontoid Fracture Fixation SystemDecember 19, 2014
K142150AIS MODULIFT VBR SYSTEMOctober 29, 2014
K133802AIS MODULIFT VBR SYSTEMApril 17, 2014
K122783PLASMAFIT ACETABULAR CUP AND VITELENE INSERTOctober 30, 2013
K130887S4C NAVIGATION INSTRUMENTSAugust 13, 2013
K123909AESCULAP CESPACE XPApril 15, 2013
K130291S4 SPINAL SYSTEMApril 11, 2013
K122985COLUMBUS REVISION KNEE SYSTEMOctober 26, 2012
K112551S4 SPINAL SYSTEMNovember 21, 2011
K101281VEGA KNEE SYSTEMJuly 30, 2010
K100147S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEMJuly 23, 2010
K083186AESCULAP HYDROLIFT VBR SYSTEMMarch 4, 2010
K090375ORTHOPILOT NEXT GENERATION-UKA SOFTWARE, MODEL FS210June 23, 2009
K083772COLUMBUS REVISION KNEE SYSTEMJune 4, 2009
K090354LAMINOPLASTY PLATING SYSTEMMay 12, 2009
K080547ORTHOPILOT NEXT GENERATION, MODEL FS101-FS106May 23, 2008
K080584METHA SHORT STEM HIP SYSTEMMay 9, 2008
K070178AESCULAP RESORBABLE PIN, MODEL FR735April 30, 2007