Spineology, Inc. · Class II · Cleared Jul 14, 2016
| K-number | K160906 |
| Device name | Rampart O Lumbar Interbody Fusion Device, Rampart T Lumbar Interbody Fusion Device, Rampart A lumbar Interbody Fusion Device |
| Applicant | Spineology, Inc. |
| Product code | MAX |
| Device class | Class II |
| Decision date | Jul 14, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 888.3080 |
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