Renovis Surgical Technologies

FDA Filings

This page includes the latest FDA filings for Renovis Surgical Technologies. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMN K190122 Renovis Surgical Technologies	Renovis A200 PS Knee System As Part Of The Renovis A200 Knee System	2019-06-20
PMN K182007 Renovis Surgical Technologies	Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System	2018-12-07
PMN K181655 Renovis Surgical Technologies	Renovis S180 Lateral Lumbar Interbody Fusion System	2018-09-11
PMN K171543 Renovis Surgical Technologies	Renovis Surgical Hip Replacement System	2017-11-16
PMN K170888 Renovis Surgical Technologies	Renovis S141 Lumbar Interbody Fusion System	2017-08-08
PMN K153250 RENOVIS SURGICAL TECHNOLOGIES	Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System	2016-03-16
PMN K143126 Renovis Surgical Technologies	Renovis S141 Lumbar Interbody Cage System	2015-02-06

Similar & Related FDA Registered Companies

• Renovis Surgical Technologies Inc.
• RENOVIS SURGICAL TECHNOLOGIES, LLC