# fda_510k (us_fda)

FDA 510(k) clearance for GenesisX Robotic Magnetic Navigation System. Latest generation endovascular surgical robotics.

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing date: 2024-01-01
- Decision date: 2024-01-01
- Verification posture: verified

## Applicant

- [Stereotaxis](/companies/stereotaxis.md)

## Covered models (1)

- [Genesis RMN / GenesisX](/models/stereotaxis-genesis.md)

## Sources (1)

- [https://ir.stereotaxis.com/news-releases/news-release-details/genesisx-robotic-magnetic-navigation-system-receives-us-fda](https://ir.stereotaxis.com/news-releases/news-release-details/genesisx-robotic-magnetic-navigation-system-receives-us-fda)

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