# New Standard Device Dba Metalogix

- Location (FDA's records): San Antonio, TX
- FDA decisions: 2 (2019–2024): 2 510(k) clearances
- Product codes: KTT (2)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Small Bone Innovations, Inc.: 1 (https://510kreport.com/company/small-bone-innovations)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)
- Orthofix, Inc.: 1 (https://510kreport.com/company/orthofix)
- Smith & Nephew, Inc., Orthopaedic Div.: 1 (https://510kreport.com/company/smith-nephew-orthopaedic-div)
- DePuy Orthopaedics, Inc.: 1 (https://510kreport.com/company/depuy-orthopaedics)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Ascension Orthopedic: 1 (https://510kreport.com/company/ascension-orthopedic)

## Its most-cited devices
- K181630: Revolution External Plating System (2019), cited by 1

## Recent decisions
- K233025: Revolution External Plating System (May 30, 2024)
- K181630: Revolution External Plating System (May 29, 2019)

Source page: https://510kreport.com/company/new-standard-device-dba-metalogix