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 |