# Spinemed Ges.M.B.H

- Location (FDA's records): Wien, AT
- FDA decisions: 1 (2018–2018): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 1 (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
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)

## Recent decisions
- K171151: ACRON™ TLIF System (Apr 27, 2018)

Source page: https://510kreport.com/company/spinemed-ges-mbh