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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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