Regulatory filing

K210989 (us_fda)

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

fda 510k · cleared · decided 2021-06-01

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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

Covered models (1)

Cirq

Sources (1)

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210989

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Identity

b91146af-1ba8-4443-b3c1-aa7ccc541ba8