Renovis Surgical Technologies - FDA 510(k) Cleared Devices
Recent clearances: Renovis A200 PS Knee System as part of the Renovis A200 Knee System, Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System, Renovis S180 Lateral Lumbar Interbody Fusion System
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Renovis Surgical Technologies Orthopedic ✕
7 devices
Cleared
Jun 20, 2019
Renovis A200 PS Knee System as part of the Renovis A200 Knee System
Orthopedic
146d
Cleared
Dec 07, 2018
Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System
Orthopedic
133d
Cleared
Sep 11, 2018
Renovis S180 Lateral Lumbar Interbody Fusion System
Orthopedic
81d
Cleared
Nov 16, 2017
Renovis Surgical Hip Replacement System
Orthopedic
174d
Cleared
Aug 08, 2017
Renovis S141 Lumbar Interbody Fusion System
Orthopedic
134d
Cleared
Mar 16, 2016
Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System
Orthopedic
128d
Cleared
Feb 06, 2015
Renovis S141 Lumbar Interbody Cage System
Orthopedic
98d