Renovis Surgical Technologies, LLC
Renovis Surgical Technologies, LLC holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2014.
Top product codes for Renovis Surgical Technologies, LLC
Recent clearances by Renovis Surgical Technologies, LLC
- K132312 — RENOVIS TESERA TRABECULAR TECHNOLOGY (T3) ACETABULAR SHELL SYSTEM
- K131354 — RENOVIS BIPOLAR HIP SYSTEM
- K131122 — S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
- K120038 — A200 KNEE SYSTEM
- K112897 — RENOVIS SURGICAL HIP JOINT REPLACEMENT PROSTHESIS
- K111940 — S 100 PEDICLE SCREW SYSTEM
- K113084 — RENOVIS CANNULATED SCREW SYSTEM
- K110965 — RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEM
- K101682 — S 100 PEDICLE SCREW SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.