Spinevision S.A.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 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 |
| 510(k) | K130302 | SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. POLYAXIAL PEDICLE SCREW FIXAT | MNI | 2013-07-30 | View |
| 510(k) | K112607 | SPINEVISION LUMIS(TM) CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S.(TM) POLYAXIAL PEDICLE ... | NKB | 2012-06-07 | View |
No matching devices.
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