# Konigsee Implantate GmbH

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2011–2011): 1 510(k) clearance
- Product codes: MQP (1)
- Predicates its devices cite: 3 (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
- Innvotec Surgical, Inc.: 1 (https://510kreport.com/company/innvotec-surgical)
- Aesculap Implant System, Inc.: 1 (https://510kreport.com/company/aesculap-implant-system)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)

## Recent decisions
- K110153: SFC Vertebral Body Replacement (Oct 12, 2011)

Source page: https://510kreport.com/company/konigsee-implantate