# Extraortho, Inc.

- Location (FDA's records): Alexandria, VA
- FDA decisions: 2 (2011–2012): 2 510(k) clearances
- Product codes: KTT (2)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 6 (1 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
- Qfx Technologies, Inc.: 2 (https://510kreport.com/company/qfx-technologies)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Smith & Nephew, Inc.: 2 (https://510kreport.com/company/smith-nephew)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)

## Firms that cite its devices most
- Zimmer, Inc.: 4 (https://510kreport.com/company/zimmer)
- Austin Miller Trauma, LLC: 1 (https://510kreport.com/company/austin-miller-trauma)

## Its most-cited devices
- K113383: Xtrafix External Fixation System (2012), cited by 5
- K111155: Xtrafix External Fixation System (2011), cited by 1

## Recent decisions
- K113383: Xtrafix External Fixation System (Jun 26, 2012)
- K111155: Xtrafix External Fixation System (Oct 20, 2011)

Source page: https://510kreport.com/company/extraortho