Medtronic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae, Retrograde Coronary Sinus Perfusion Cannulae, Clearview Intracoronary Shunts
209
Total
208
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medtronic, Inc. Orthopedic ✕
5 devices
Cleared
May 27, 2021
LigaPASS® Spinal System, CD Horizon™ Spinal System
Orthopedic
48d
Cleared
Feb 27, 2017
Kyphon Xpede Bone Cement
Orthopedic
119d
Cleared
Aug 24, 2016
Kyphon HV-R Bone Cement
Orthopedic
139d
Cleared
Jul 23, 2015
KYPHON ELEMENT Inflatable Bone Tamp
Orthopedic
45d
Cleared
Aug 12, 2010
KYPH X HV-R BONE CEMENT
Orthopedic
241d