# Orthospin

- Location (FDA's records): Misgav, IL
- FDA decisions: 2 (2019–2021): 2 510(k) clearances
- Names in FDA's records: Orthospin (1); Orthospin, Ltd. (1)
- Product codes: KTT (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 3 (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
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Firms that cite its devices most
- DePuy Synthes: 1 (https://510kreport.com/company/depuy-synthes)
- Synthes (USA) Products, LLC: 1 (https://510kreport.com/company/synthes-usa-products)

## Its most-cited devices
- K202810: AutoStrut G2 (2021), cited by 2
- K191241: AutoStrut (2019), cited by 1

## Recent decisions
- K202810: AutoStrut G2 (Jan 6, 2021)
- K191241: AutoStrut (Aug 14, 2019)

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