# Calvary Spine, LLC

- Location (FDA's records): Round Rock, TX
- FDA decisions: 2 (2008–2020): 2 510(k) clearances
- Product codes: MAX (1), NKB (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- Renovis Surgical Technologies, LLC: 1 (https://510kreport.com/company/renovis-surgical-technologies)

## Firms that cite its devices most
- Spinenet, LLC: 1 (https://510kreport.com/company/spinenet)
- Renovis Surgical Technologies, LLC: 1 (https://510kreport.com/company/renovis-surgical-technologies)

## Its most-cited devices
- K082260: Integra Cervical and Petra Plif Lumbar Cages (2008), cited by 2

## Recent decisions
- K201568: Calvary Spine Pedicle Screw System (Nov 12, 2020)
- K082260: Integra Cervical and Petra Plif Lumbar Cages (Oct 17, 2008)

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