# Laura Cattabriga

- Location (FDA's records): N. Bay Village, FL
- FDA decisions: 2 (2014–2014): 2 510(k) clearances
- Product codes: HRS (1), HWC (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (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
- Internal Fixation Systems, Inc.: 3 (https://510kreport.com/company/internal-fixation-systems)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Firms that cite its devices most
- Orthonovis, Inc.: 2 (https://510kreport.com/company/orthonovis)

## Its most-cited devices
- K130614: Bone Fragment and Fixation Plates, Screws and Washers (2014), cited by 1
- K130613: Cannulated Screw and Kirschner (Kwire) System (2014), cited by 1

## Recent decisions
- K130613: Cannulated Screw and Kirschner (Kwire) System (Jan 22, 2014)
- K130614: Bone Fragment and Fixation Plates, Screws and Washers (Jan 17, 2014)

Source page: https://510kreport.com/company/laura-cattabriga
