Renovis Surgical Technologies
Renovis Surgical Technologies holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2019.
Top product codes for Renovis Surgical Technologies
Recent clearances by Renovis Surgical Technologies
- K190122 — Renovis A200 PS Knee System as part of the Renovis A200 Knee System
- K182007 — Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System
- K181655 — Renovis S180 Lateral Lumbar Interbody Fusion System
- K171543 — Renovis Surgical Hip Replacement System
- K170888 — Renovis S141 Lumbar Interbody Fusion System
- K153250 — Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System
- K143126 — Renovis S141 Lumbar Interbody Cage System
Data sourced from openFDA. This site is unofficial and independent of the FDA.