# Acme Spine, LLC

- Location (FDA's records): Riverside, CA
- FDA decisions: 2 (2000–2007): 2 510(k) clearances
- Product codes: MNH (1), MNI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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 that cite its devices most
- Black Box Medical: 2 (https://510kreport.com/company/black-box-medical)
- Spine360: 2 (https://510kreport.com/company/spine360)
- Torrey Spine: 1 (https://510kreport.com/company/torrey-spine)
- R&D Innovation, LLC: 1 (https://510kreport.com/company/r-d-innovation)
- Spineworks, LLC: 1 (https://510kreport.com/company/spineworks)

## Its most-cited devices
- K071824: Acme Talon Pedicle Screw (2007), cited by 6
- K001044: Acme Spine System - Series 6000, 7000, Monoaxial and Polyaxial Screw System (2000), cited by 1

## Recent decisions
- K071824: Acme Talon Pedicle Screw (Sep 4, 2007)
- K001044: Acme Spine System - Series 6000, 7000, Monoaxial and Polyaxial Screw System (Nov 3, 2000)

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