# Orthopaedic Designs, Inc.

- Location (FDA's records): Alexandria, VA
- FDA decisions: 2 (1988–1997): 2 510(k) clearances
- Product codes: HSB (1), KTT (1)
- 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
- Howmedica Corp.: 6 (https://510kreport.com/company/howmedica)
- Depuy, Inc.: 2 (https://510kreport.com/company/depuy)
- Pfizer, Inc.: 1 (https://510kreport.com/company/pfizer)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Recent decisions
- K971993: Odi Compression Hip Screw System (Nov 12, 1997)
- K880737: Self Guiding  (SG) Interlocking Nail (Mar 14, 1988)

Source page: https://510kreport.com/company/orthopaedic-designs