# Musculoskeletal Clinical Regulatory Advisers

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: ODP (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 5 (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
- Us Spine: 1 (https://510kreport.com/company/us-spine)
- Interbody Innovations, Llp: 1 (https://510kreport.com/company/interbody-innovations)
- Scient'X USA, Inc.: 1 (https://510kreport.com/company/scient-x-usa)
- Ldr Spine USA: 1 (https://510kreport.com/company/ldr-spine-usa)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Spineart: 1 (https://510kreport.com/company/spineart)

## Firms that cite its devices most
- SeaSpine Orthopedics Corporation: 3 (https://510kreport.com/company/seaspine-orthopedics)
- Medacta International S.A.: 1 (https://510kreport.com/company/medacta-international)
- Theken Spine, LLC: 1 (https://510kreport.com/company/theken-spine)

## Its most-cited devices
- K101363: VU Cpod Intervertebral Bodu Fusion Device (2010), cited by 5

## Recent decisions
- K101363: VU Cpod Intervertebral Bodu Fusion Device (Dec 16, 2010)

Source page: https://510kreport.com/company/musculoskeletal-clinical-regulatory-advisers