# Trinity Orthopedics, LLC

- Location (FDA's records): San Diego, CA
- FDA decisions: 2 (2007–2008): 2 510(k) clearances
- Product codes: MNI (2)
- Predicates its devices cite: 10 (0 its own); citations of its devices by later devices: 0 (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
- Depuy, Inc.: 3 (https://510kreport.com/company/depuy)
- Stryker Spine: 3 (https://510kreport.com/company/stryker-spine)
- Depuyacromed: 1 (https://510kreport.com/company/depuyacromed)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)
- Sofamor Danek USA,Inc.: 1 (https://510kreport.com/company/sofamor-danek-usa)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)

## Recent decisions
- K081790: Modification to Single Planar Multi Axis (Spma) Pedicle Screw System (Jul 24, 2008)
- K070295: Single Planar Multi Axial (Spma) Pedicle Screw System (May 21, 2007)

Source page: https://510kreport.com/company/trinity-orthopedics