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 |