510(k) K210989 ยท HAW Neurological Stereotaxic Instrument
Cirq, Cirq Robotic Alignment System, Cirq Robotic Alignment Module Cranial, Cirq Robotic Alignment Module, Cirq Robotic Alignment Cranial And Spine, CIRQ Robotic Alignment Cranial and Spine System
| Applicant | Brainlab AG, Munich, DE |
| Decision | Substantially Equivalent, Nov 12, 2021 |
| Received | Apr 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210989
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.