# Interbody Innovations, Llp

- Location (FDA's records): Round Rock, TX
- FDA decisions: 4 (2005–2008): 4 510(k) clearances
- Product codes: NVR (2), ODP (1), JDK (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 10 (1 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
- Medtronic Sofamor Danek: 2 (https://510kreport.com/company/medtronic-sofamor-danek)
- Spinal Concepts, Inc.: 1 (https://510kreport.com/company/spinal-concepts)
- Spine Next SA: 1 (https://510kreport.com/company/spine-next)
- Signus Medical, LLC: 1 (https://510kreport.com/company/signus-medical)

## Firms that cite its devices most
- Amendia, Inc.: 2 (https://510kreport.com/company/amendia)
- Corelink, LLC: 1 (https://510kreport.com/company/corelink)
- Musculoskeletal Clinical Regulatory Advisers: 1 (https://510kreport.com/company/musculoskeletal-clinical-regulatory-advisers)
- Titan Spine, LLC: 1 (https://510kreport.com/company/titan-spine)
- Eminent Spine: 1 (https://510kreport.com/company/eminent-spine)
- Nanovis, LLC: 1 (https://510kreport.com/company/nanovis)
- Altus Partners, LLC: 1 (https://510kreport.com/company/altus-partners)
- Curiteva, Inc.: 1 (https://510kreport.com/company/curiteva)

## Its most-cited devices
- K081614: Zeus Small Cervical Cage and Large, Extra Large, Curved and Straight Lumbar Cages (2008), cited by 9
- K062992: Spinal Spheres (2007), cited by 1

## Recent decisions
- K081614: Zeus Small Cervical Cage and Large, Extra Large, Curved and Straight Lumbar Cages (Sep 5, 2008)
- K073105: Peek Spinal Spheres (Jan 3, 2008)
- K062992: Spinal Spheres (Jul 27, 2007)
- K051371: Interbody Innovations Cement Restrictor (Dec 6, 2005)

Source page: https://510kreport.com/company/interbody-innovations