# Camber Spine

- Location (FDA's records): Newtown Square, PA
- FDA decisions: 4 (2014–2015): 4 510(k) clearances
- Product codes: MAX (1), ODP (1), MQP (1), NKB (1)
- Predicates its devices cite: 10 (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
- Globus Medical, Inc.: 4 (https://510kreport.com/company/globus-medical)
- Corelink, LLC: 2 (https://510kreport.com/company/corelink)
- Camber Spine Technologies: 1 (https://510kreport.com/company/camber-spine-technologies)
- Nexxt Spine, LLC: 1 (https://510kreport.com/company/nexxt-spine)
- Spinal Elements, Inc.: 1 (https://510kreport.com/company/spinal-elements)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)

## Firms that cite its devices most
- Camber Spine Technologies: 5 (https://510kreport.com/company/camber-spine-technologies)
- The Institute of Musculoskeletal Science & Education: 1 (https://510kreport.com/company/institute-of-musculoskeletal-science-education)

## Its most-cited devices
- K133529: Camber Spine Coveris Cervical Cage (2014), cited by 3
- K134038: Camber Spine Diagon Oblique Cage (2014), cited by 1
- K143490: VERTA Corpectomy Cage (2015), cited by 1
- K133366: Orthros Posterior Stabilization System (2014), cited by 1

## Recent decisions
- K143490: VERTA Corpectomy Cage (Jan 26, 2015)
- K133366: Orthros Posterior Stabilization System (Apr 8, 2014)
- K134038: Camber Spine Diagon Oblique Cage (Mar 20, 2014)
- K133529: Camber Spine Coveris Cervical Cage (Mar 20, 2014)

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