The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Cd Horizon® Spinal System, Medtronic Reusable Instruments For Use With The Ipc® Powerease® System, Medtronic Navigated Reusable Instruments For Use With The Stealthstation® And Ipc® Powerease® Systems.
| Device ID | K170679 | 
| 510k Number | K170679 | 
| Device Name: | CD HORIZON® Spinal System, Medtronic Reusable Instruments For Use With The IPC® POWEREASE® System, Medtronic Navigated Reusable Instruments For Use With The STEALTHSTATION® And IPC® POWEREASE® Systems | 
| Classification | Thoracolumbosacral Pedicle Screw System | 
| Applicant | Medtronic Sofamor Danek 1800 Pyramid Place Memphis, TN 38132 | 
| Contact | Kanesha Hines | 
| Correspondent | Kanesha Hines Medtronic Sofamor Danek 1800 Pyramid Place Memphis, TN 38132 | 
| Product Code | NKB | 
| Subsequent Product Code | HWE | 
| Subsequent Product Code | KWP | 
| Subsequent Product Code | KWQ | 
| Subsequent Product Code | OLO | 
| CFR Regulation Number | 888.3070 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2017-03-06 | 
| Decision Date | 2017-05-11 | 
| Summary: | summary | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  CD HORIZON  75079759  2108361 Live/Registered | WARSAW ORTHOPEDIC, INC. 1996-03-28 |