Spinevision S.A.

5 FDA 510(k) medical device clearances.

Top product codes for Spinevision S.A.

Recent clearances by Spinevision S.A.

K153783 — SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF MAX · 2016-05-04
K160124 — LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System MNI · 2016-04-04
K133575 — SPINEVISION LUMIS CANNULATED PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. PEDICLE SCREW FIXATION SYSTEM MNH · 2014-06-30
K130302 — SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. POLYAXIAL PEDICLE SCREW FIXAT MNI · 2013-07-30
K112607 — SPINEVISION LUMIS(TM) CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S.(TM) POLYAXIAL PEDICLE ... NKB · 2012-06-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.