Kyphon V™ Premium Vertebroplasty Kit 13Ga - SFDA Registration ME0000000280SFDAA00063
Access comprehensive regulatory information for Kyphon V™ Premium Vertebroplasty Kit 13Ga in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000000280SFDAA00063 and manufactured by Medtronic Sofamor Danek USA, Inc..
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
Vertebral and Extremity Fracture Device
The KYPHON V™ Vertebroplasty Kit is intended for percutaneous access to bone and the delivery of bone cement, including during kyphoplasty or vertebroplasty procedures.
[]