# Cardinal Spine, LLC

- Location (FDA's records): San Diego, CA
- FDA decisions: 4 (2011–2016): 4 510(k) clearances
- Product codes: MQP (2), PLR (1), ODP (1)
- Predicates its devices cite: 12 (3 its own); citations of its devices by later devices: 8 (3 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
- Depuyacromed: 2 (https://510kreport.com/company/depuyacromed)
- Ldr Spine USA: 2 (https://510kreport.com/company/ldr-spine-usa)
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)
- Pioneer Surgical Technology: 1 (https://510kreport.com/company/pioneer-surgical-technology)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)

## Firms that cite its devices most
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)
- MiRus, LLC: 1 (https://510kreport.com/company/mirus)
- K2m, Inc.: 1 (https://510kreport.com/company/k2m)
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)
- Coligne AG: 1 (https://510kreport.com/company/coligne)

## Its most-cited devices
- K152568: C-VBR (2016), cited by 4
- K121176: STGC (2012), cited by 2
- K142030: STGC-Lordotic (2015), cited by 1
- K100698: STCC (2011), cited by 1

## Recent decisions
- K152568: C-VBR (Feb 11, 2016)
- K142030: STGC-Lordotic (Jan 23, 2015)
- K121176: STGC (Aug 17, 2012)
- K100698: STCC (Mar 14, 2011)

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