Medtronic Navigation - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Medtronic Navigation has 9 FDA 510(k) cleared medical devices. Based in Louisville, US.
Latest FDA clearance: May 2025. Active since 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medtronic Navigation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medtronic Navigation
9 devices
Cleared
May 29, 2025
Visualase V2 MRI-guided Laser Ablation System (9736422)
Neurology
115d
Cleared
Dec 22, 2021
StealthStation S8 Cranial v2.0
Neurology
142d
Cleared
Jul 08, 2021
StealthStation Spinous Process Clamps
Orthopedic
59d
Cleared
Jun 18, 2020
NavLock Trackers
Orthopedic
30d
Cleared
Mar 24, 2020
PlasmaBlade X 3.0S LIGHT
General & Plastic Surgery
92d
Cleared
Nov 02, 2018
NavLock Trackers, Robotic Reference Frame
Orthopedic
91d
Cleared
Jul 11, 2018
Ziehm RFD 3D Tracker
Orthopedic
104d
Cleared
Jul 03, 2017
NavLock Trackers
Orthopedic
63d
Cleared
May 01, 2017
StealthStation S8 Spine Software v1.0.0
Orthopedic
118d