Spineex, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2020-04-30
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K200816 | SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices | MAX | 2020-04-30 | View |
| 510(k) | K190193 | SpineEX Sagittae® Lateral Lumbar Interbody Fusion Devices | MAX | 2019-03-04 | View |
| 510(k) | K181531 | SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices | MAX | 2018-10-05 | View |
No matching devices.