510(k) K221618 ยท OLO Orthopedic Stereotaxic Instrument
Spine & Trauma Navigation, Spine Navigation, Navigation Software Spine & Trauma, Alignment System Spine, Alignment Software Spine, Cirq Arm System
| Applicant | Brainlab AG, Munich, DE |
| Decision | Substantially Equivalent, Aug 30, 2022 |
| Received | Jun 3, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221618
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.