Camber Spine Technologies, LLC - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Camber Spine Technologies, LLC has 6 FDA 510(k) cleared medical devices. Based in Wayne, US.
Latest FDA clearance: Apr 2024. Active since 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Camber Spine Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Camber Spine Technologies, LLC
6 devices
Cleared
Apr 16, 2024
Alcantara Thoracolumbar Plate System
Orthopedic
263d
Cleared
Sep 02, 2022
Camber Sacroiliac (SI) Fixation System
Orthopedic
641d
Cleared
Jun 15, 2021
SPIRA-T Oblique Posterior Lumbar Spacers, SPIRA-P Posterior Lumbar Spacers
Orthopedic
106d
Cleared
Oct 22, 2019
FORTICO Anterior Cervical Fixation System
Orthopedic
130d
Cleared
Oct 27, 2018
ORTHROS™ Posterior Stabilization System
Orthopedic
197d
Cleared
Jun 25, 2018
SPIRA Open Matrix LLIF
Orthopedic
97d