# Artos Medical Products GmbH

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 4 (1996–1996): 4 510(k) clearances
- Product codes: JDI (2), LWJ (2)
- Predicates its devices cite: 0 (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

## Recent decisions
- K962034: SC, Cementless Hip System (Oct 23, 1996)
- K962268: Chrome Cobalt Ball Head (Oct 23, 1996)
- K962086: CPS, Cemented Cup System (Aug 7, 1996)
- K961899: CPS, Cemented Hip System (Aug 1, 1996)

Source page: https://510kreport.com/company/artos-medical-products