Captiva Spine, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K193270 | CapLOX II®/TowerLOX® MIS Pedicle Screw System | NKB | 2020-01-31 | View |
| 510(k) | K181229 | TirboLOX-C Cervical IBFD | ODP | 2018-09-19 | View |
| 510(k) | K180990 | TirboLOX-L Lumbar IBFD | MAX | 2018-08-13 | View |
| 510(k) | K180475 | CapLOX II® / TowerLOX® MIS Pedicle Screw System | NKB | 2018-03-19 | View |
| 510(k) | K120292 | CAPLOX II PEDICLE SCREW SYSTEM | MNI | 2012-04-13 | View |
| 510(k) | K111115 | CAPTIVA SPINE CAPLOX II SPINAL FIXATION SYSTEM | MNI | 2011-09-13 | View |
| 510(k) | K110585 | CAPTIVA SPINE FUSELOX CERVICAL CAGE | ODP | 2011-03-25 | View |
| 510(k) | K092017 | PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD) | MAX | 2009-12-01 | View |
No matching devices.
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