The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc with the FDA for Atlantis Anterior Cervical Plate System.
| Device ID | K152623 |
| 510k Number | K152623 |
| Device Name: | ATLANTIS Anterior Cervical Plate System |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | MEDTRONIC SOFAMOR DANEK USA, INC 1800 PYRAMID PLACE Memphis, TN 38132 |
| Contact | Laveeda Leflore |
| Correspondent | Laveeda Leflore MEDTRONIC SOFAMOR DANEK USA, INC 1800 PYRAMID PLACE Memphis, TN 38132 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-14 |
| Decision Date | 2015-11-12 |
| Summary: | summary |