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Spinevision S.A.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest Approval2016-05-04
TypeNumberDevice NameCodeDate
510(k) K153783 SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF MAX 2016-05-04 View
510(k) K160124 LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System MNI 2016-04-04 View