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. Neurology ✕
5 devices
Cleared
May 26, 2020
Exacta External Drainage and Monitoring System, Exacta Pole with Laser Level,...
Neurology
29d
Cleared
Apr 09, 2020
Medtronic External Drainage and Monitoring System, Medtronic External...
Neurology
30d
Cleared
Mar 26, 2020
Becker External Drainage and Monitoring System
Neurology
30d
Cleared
Oct 26, 2010
MULTI-LEAD TRIALING CABLE MODEL 355531
Neurology
54d
Cleared
Aug 16, 2006
MODEL 3875 1 X 8 SC TEST STIMULATION LEAD
Neurology
28d