Nu Vasive, Incorporated · Class II · Cleared Feb 8, 2018
| K-number | K173025 |
| Device name | NuVasive® MLX® Medial Lateral Expandable Lumbar Interbody System; NuVasive® AP Expandable XLIF System |
| Applicant | Nu Vasive, Incorporated |
| Product code | MAX |
| Device class | Class II |
| Decision date | Feb 8, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 888.3080 |
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