The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Cd Horizon Spinal System.
| Device ID | K090390 | 
| 510k Number | K090390 | 
| Device Name: | CD HORIZON SPINAL SYSTEM | 
| Classification | Thoracolumbosacral Pedicle Screw System | 
| Applicant | MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 | 
| Contact | Melisa Lansky | 
| Correspondent | Melisa Lansky 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 | 
| CFR Regulation Number | 888.3070 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Special | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2009-02-17 | 
| Decision Date | 2009-05-15 | 
| Summary: | summary |