The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Mlx - Medial Lateral Expandable Lumbar Interbody System.
| Device ID | K140770 |
| 510k Number | K140770 |
| Device Name: | MLX - MEDIAL LATERAL EXPANDABLE LUMBAR INTERBODY SYSTEM |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | NUVASIVE, INCORPORATED 7475 LUSK BLVD San Diego, CA 92121 |
| Contact | Olga Lewis |
| Correspondent | Olga Lewis NUVASIVE, INCORPORATED 7475 LUSK BLVD San Diego, CA 92121 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-03-27 |
| Decision Date | 2014-07-25 |
| Summary: | summary |