# K210989 (us_fda)

FDA 510(k) K210989 for Brainlab CIRQ Robotic Alignment System. Neurological stereotaxic instrument.

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K210989
- Filing date: 2021-01-01
- Decision date: 2021-06-01
- Verification posture: verified

## Applicant

- [Brainlab](/companies/brainlab.md)

## Covered models (1)

- [Cirq](/models/brainlab-cirq.md)

## Sources (1)

- [https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210989](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210989)

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