K234047
- 510(k) number
- K234047
- Device name
- Automatic Registration
- Applicant
- Brainlab AG DE
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2024-03-20
- Date received
- 2023-12-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K234047.pdf
Official FDA record: K234047
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.