# Djo Surgical

- Location (FDA's records): Austin
- FDA decisions: 2 (2003–2009): 1 510(k) clearance and 1 original PMA approval
- Product codes: MRA (1), PHX (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 11 (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
- Encore Medical L.P.: 2 (https://510kreport.com/company/encore-medical)

## Firms that cite its devices most
- Encore Medical L.P.: 5 (https://510kreport.com/company/encore-medical)
- Tornier, Inc.: 2 (https://510kreport.com/company/tornier)
- Lima Corporate S.P.A.: 2 (https://510kreport.com/company/lima-corporate)
- Materialise NV: 1 (https://510kreport.com/company/materialise)
- Djo Global: 1 (https://510kreport.com/company/djo-global)

## Its most-cited devices
- K092873: Reverse Shoulder Prosthesis (2009), cited by 11

## Recent decisions
- K092873: Reverse Shoulder Prosthesis (Oct 27, 2009)
- N980003: Keramos Ceramic/Ceramic Total Hip System (Nov 26, 2003)

Source page: https://510kreport.com/company/djo-surgical