Renovis Surgical Technologies, LLC
FDA 510(k) medical device clearances.
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.