# Nutek Orthopaedics, Inc.

- Location (FDA's records): Ft. Lauderdale, FL
- FDA decisions: 2 (2009–2013): 2 510(k) clearances
- Product codes: KTT (2)
- Predicates its devices cite: 4 (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
- Small Bone Innovations, Inc.: 1 (https://510kreport.com/company/small-bone-innovations)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)
- Teleflex Medical: 1 (https://510kreport.com/company/teleflex-medical)
- Gexfix USA, Inc.: 1 (https://510kreport.com/company/gexfix-usa)

## Recent decisions
- K122777: NBX - Non Bridging External Fixator Hand (May 15, 2013)
- K082833: NBX - Non-Bridging External Fixator - Shoulder (Feb 5, 2009)

Source page: https://510kreport.com/company/nutek-orthopaedics