Camber Spine Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Camber Spine Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: Alcantara Thoracolumbar Plate System, Camber Sacroiliac (SI) Fixation System, SPIRA-T Oblique Posterior Lumbar Spacers, SPIRA-P Posterior Lumbar Spacers
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.
Regulatory submissions have been managed by RQMIS, Inc., MRC Global and MRC Global, LLC.
FDA 510(k) Regulatory Record - 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