FDA 510(k) Applications Submitted by SPINEVISION, S.A.

FDA 510(k) Number Submission Date Device Name Applicant
K112607 09/07/2011 SPINEVISION LUMIS(TM) CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S.(TM) POLYAXIAL PEDICLE ... SPINEVISION, S.A.
K130302 02/07/2013 SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. POLYAXIAL PEDICLE SCREW FIXAT SPINEVISION, S.A.
K133575 11/20/2013 SPINEVISION LUMIS CANNULATED PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. PEDICLE SCREW FIXATION SYSTEM SPINEVISION, S.A.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact