Southern Spine, LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Southern Spine, LLC has 4 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Last cleared in 2021. Active since 2007. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Southern Spine, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Resources Group, Inc. as regulatory consultant.
4 devices
Cleared
Nov 16, 2021
Deploy Expandable Interbody System
Orthopedic
154d
Cleared
Aug 14, 2013
C-FUSE CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
Orthopedic
131d
Cleared
Dec 20, 2012
STABILINK MIS SPINAL FIXATION SYSTEM
Orthopedic
79d
Cleared
May 16, 2007
SOUTHERN SPINE ANTERIOR CERVICAL STABILIZATION SYSTEM, KWIK- FIX CERVICAL...
Orthopedic
147d