The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Incorporated with the FDA for Kyphon Hv-r Fenestrated Screw Cement, Cd Horizon Fenestrated Screw Set.
| Device ID | K152604 |
| 510k Number | K152604 |
| Device Name: | KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw Set |
| Classification | Bone Cement, Posterior Screw Augmentation |
| Applicant | Medtronic Sofamor Danek USA, Incorporated 1800 Pyramid Place Memphis, TN 38132 |
| Contact | Pamela Edwards |
| Correspondent | Lee Grant Medtronic Sofamor Danek USA, Incorporated 1800 Pyramid Place Memphis, TN 38132 |
| Product Code | PML |
| CFR Regulation Number | 888.3027 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-11 |
| Decision Date | 2016-01-06 |
| Summary: | summary |