Renovis Surgical Technologies, Inc.
Renovis Surgical Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2018.
Top product codes for Renovis Surgical Technologies, Inc.
Recent clearances by Renovis Surgical Technologies, Inc.
- K180502 — S128 Anterior Lumbar Interbody Fusion (ALIF) System
- K152193 — Renovis Anterior Cervical Plate System
- K143647 — Renovis Surgical Hip Replacement System
- K141676 — RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM
- K142095 — RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
- K141370 — RENOVIS CEMENTED HIP SYSTEM
- K140106 — S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.