FDA 510(k) Applications Submitted by RENOVIS SURGICAL TECHNOLOGIES, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K112897 10/03/2011 RENOVIS SURGICAL HIP JOINT REPLACEMENT PROSTHESIS RENOVIS SURGICAL TECHNOLOGIES, LLC
K113084 10/18/2011 RENOVIS CANNULATED SCREW SYSTEM RENOVIS SURGICAL TECHNOLOGIES, LLC
K110965 04/06/2011 RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEM RENOVIS SURGICAL TECHNOLOGIES, LLC
K101682 06/15/2010 S 100 PEDICLE SCREW SYSTEM RENOVIS SURGICAL TECHNOLOGIES, LLC
K111940 07/08/2011 S 100 PEDICLE SCREW SYSTEM RENOVIS SURGICAL TECHNOLOGIES, LLC
K120038 01/05/2012 A200 KNEE SYSTEM RENOVIS SURGICAL TECHNOLOGIES, LLC
K131122 04/22/2013 S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM RENOVIS SURGICAL TECHNOLOGIES, LLC
K132312 07/25/2013 RENOVIS TESERA TRABECULAR TECHNOLOGY (T3) ACETABULAR SHELL SYSTEM RENOVIS SURGICAL TECHNOLOGIES, LLC


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