The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa with the FDA for Cd Horizon™ Fenestrated Screw Set.
| Device ID | K170347 |
| 510k Number | K170347 |
| Device Name: | CD HORIZON™ Fenestrated Screw Set |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Medtronic Sofamor Danek USA 1800 Pyramid Place Memphis, TN 38132 |
| Contact | Lee Grant |
| Correspondent | Lee Grant Medtronic Sofamor Danek USA 1800 Pyramid Place Memphis, TN 38132 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-02-03 |
| Decision Date | 2017-04-04 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CD HORIZON 75079759 2108361 Live/Registered |
WARSAW ORTHOPEDIC, INC. 1996-03-28 |