Spectranetics, Inc. - FDA 510(k) Cleared Devices
17
Total
16
Cleared
1
Denied
Spectranetics, Inc. has 16 FDA 510(k) cleared cardiovascular devices. Based in Colorado Springs, US.
Last cleared in 2022. Active since 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Spectranetics, Inc.
17 devices
Cleared
Dec 15, 2022
TightRail Guardian Motorized Dilator Sheath, 9 French (575-009)
Cardiovascular
28d
Cleared
Dec 08, 2022
Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser...
Cardiovascular
79d
Cleared
Aug 24, 2022
TightRail Guardian Motorized Dilator Sheath
Cardiovascular
357d
Not Cleared
Dec 21, 2021
CavaClear Laser Sheath
Cardiovascular
179d
Cleared
Dec 23, 2020
Bridge Occlusion Balloon
Cardiovascular
20d
Cleared
Apr 05, 2018
Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser...
Cardiovascular
20d
Cleared
Nov 27, 2017
Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser...
Cardiovascular
82d
Cleared
Apr 07, 2017
Spectranetics Turbo-Elite Laser Atherectomy Catheters
Cardiovascular
91d
Cleared
Jan 05, 2017
Turbo-Power (2.0mm) Laser Atherectomy Catheters
Cardiovascular
113d
Cleared
Jul 08, 2016
TightRail Sub-C Rotating Dilator Sheath
Cardiovascular
57d
Cleared
Feb 05, 2016
Bridge Occlusion Balloon
Cardiovascular
58d
Cleared
Nov 12, 2015
Turbo-Power Laser Atherectomy Catheter
Cardiovascular
100d