This page includes the latest FDA filings for Spinevision S A. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
SpineVision S.A. | SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF | 2016-05-04 |
SpineVision S.A. | LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System | 2016-04-04 |
SPINEVISION, S.A. | SPINEVISION LUMIS CANNULATED PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. PEDICLE SCREW FIXATION SYSTEM | 2014-06-30 |
SPINEVISION, S.A. | SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. POLYAXIAL PEDICLE SCREW FIXAT | 2013-07-30 |
SPINEVISION, S.A. | SPINEVISION LUMIS(TM) CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S.(TM) POLYAXIAL PEDICLE ... | 2012-06-07 |
SEC | 0001222454 | SPINEVISION SA |