FDA 510(k) Applications Submitted by SpineVision S.A.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160124 | 01/20/2016 | LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System | SpineVision S.A. |
| K153783 | 12/31/2015 | SpaceVision« PLIF, SpaceVision« OLIF, SpaceVision« TLIF | SpineVision S.A. |
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