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 |