Choicespine, LP is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Choicespine, LP - FDA 510(k) Cleared Devices
Recent clearances: Boomerang™ Anterior Cervical Plate System, ChoiceSpine Stealth Cervical Spacer System, Choice Spine Navigation System
22
Total
22
Cleared
0
Denied
Choicespine, LP has 22 FDA 510(k) cleared orthopedic devices. Based in Chesterland, US.
Historical record: 22 cleared submissions from 2008 to 2019.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Choicespine, LP
22 devices
Cleared
May 01, 2019
Boomerang™ Anterior Cervical Plate System
Orthopedic
85d
Cleared
Mar 06, 2019
ChoiceSpine Stealth Cervical Spacer System
Orthopedic
89d
Cleared
Jan 08, 2019
Choice Spine Navigation System
Orthopedic
102d
Cleared
Jan 03, 2019
Raven Lumbar Plate System
Orthopedic
45d
Cleared
May 16, 2018
HARRIER-SA™ Lumbar Interbody System
Orthopedic
78d
Cleared
Jan 26, 2018
TiGer Shark™ System
Orthopedic
130d
Cleared
Jan 19, 2018
Choice Spine Laminoplasty™ Fixation System
Orthopedic
109d
Cleared
Oct 23, 2017
Acapella Cervical Spacer System
Orthopedic
154d
Cleared
Jun 08, 2017
ChoiceSpine™ Proliant® Posterior Pedicle Screw and Hook Fixation System
Orthopedic
80d
Cleared
Apr 26, 2017
The Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems
Orthopedic
27d
Cleared
Apr 21, 2017
Tomcat Cervical Spinal System
Orthopedic
21d
Cleared
Nov 23, 2016
Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice...
Orthopedic
117d