The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Cd Horizon Voyager Spinal System.
| Device ID | K113529 |
| 510k Number | K113529 |
| Device Name: | CD HORIZON VOYAGER SPINAL SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 |
| Contact | Mike Scott |
| Correspondent | Mike Scott MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| Subsequent Product Code | OSH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Se - With Limitations (SESU) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-11-30 |
| Decision Date | 2012-02-09 |
| Summary: | summary |