The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for Divergence-l Anterior/oblique Lumbar Fusion System.
| Device ID | K150135 |
| 510k Number | K150135 |
| Device Name: | DIVERGENCE-L Anterior/Oblique Lumbar Fusion System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
| Contact | Lila Joe |
| Correspondent | Lila Joe MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
| Product Code | MAX |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-01-21 |
| Decision Date | 2015-06-11 |
| Summary: | summary |