Medical Device Manufacturer · US , Round Rock , TX

Renovis Surgical Technologies, LLC - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2010
9
Total
9
Cleared
0
Denied

Renovis Surgical Technologies, LLC has 9 FDA 510(k) cleared medical devices. Based in Round Rock, US.

Historical record: 9 cleared submissions from 2010 to 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Renovis Surgical Technologies, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Renovis Surgical Technologies, LLC
9 devices
1-9 of 9
Cleared Apr 11, 2014
RENOVIS TESERA TRABECULAR TECHNOLOGY (T3) ACETABULAR SHELL SYSTEM
K132312 · LPH
Orthopedic · 260d
Cleared Sep 19, 2013
RENOVIS BIPOLAR HIP SYSTEM
K131354 · KWY
Orthopedic · 132d
Cleared Sep 18, 2013
S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
K131122 · OVD
Orthopedic · 149d
Cleared Feb 14, 2013
A200 KNEE SYSTEM
K120038 · OIY
Orthopedic · 406d
Cleared Jun 13, 2012
RENOVIS SURGICAL HIP JOINT REPLACEMENT PROSTHESIS
K112897 · OQG
Orthopedic · 254d
Cleared May 15, 2012
S 100 PEDICLE SCREW SYSTEM
K111940 · MNH
Orthopedic · 312d
Cleared Dec 09, 2011
RENOVIS CANNULATED SCREW SYSTEM
K113084 · HWC
Orthopedic · 52d
Cleared May 11, 2011
RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEM
K110965 · KTT
Orthopedic · 35d
Cleared Dec 07, 2010
S 100 PEDICLE SCREW SYSTEM
K101682 · MNI
Orthopedic · 175d
Filters
Filter by Specialty
All9 Orthopedic 9