# Southern Spine, LLC

- Location (FDA's records): Alpharetta, GA
- FDA decisions: 4 (2007–2021): 4 510(k) clearances
- Product codes: KWP (1), ODP (1), KWQ (1), MAX (1)
- Predicates its devices cite: 14 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Lanx, Inc.: 7 (https://510kreport.com/company/lanx)
- K2m, Inc.: 2 (https://510kreport.com/company/k2m)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Spinal Devices, LLC: 1 (https://510kreport.com/company/spinal-devices)
- Smisson-Cartledge: 1 (https://510kreport.com/company/smisson-cartledge)
- Amendia, Inc.: 1 (https://510kreport.com/company/amendia)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)

## Firms that cite its devices most
- Precision Spine, Inc.: 1 (https://510kreport.com/company/precision-spine)
- Reliance Medical Systems, LLC: 1 (https://510kreport.com/company/reliance-medical-systems)
- Atlas Spine, Inc.: 1 (https://510kreport.com/company/atlas-spine)
- Ldr Spine USA: 1 (https://510kreport.com/company/ldr-spine-usa)
- Exactech, Inc.: 1 (https://510kreport.com/company/exactech)
- Bk Meditech, Co., Ltd.: 1 (https://510kreport.com/company/bk-meditech)

## Its most-cited devices
- K123093: Stabilink Mis Spinal Fixation System (2012), cited by 3
- K130948: C-Fuse Cervical Intervertebral Body Fusion System (2013), cited by 3

## Recent decisions
- K211845: Deploy Expandable Interbody System (Nov 16, 2021)
- K130948: C-Fuse Cervical Intervertebral Body Fusion System (Aug 14, 2013)
- K123093: Stabilink Mis Spinal Fixation System (Dec 20, 2012)
- K063764: Southern Spine Anterior Cervical Stabilization System, Kwik- Fix Cervical System, and Kwik-Fix / TS Cervical System (May 16, 2007)

Source page: https://510kreport.com/company/southern-spine