K243958
- 510(k) number
- K243958
- Device name
- Consolidated Operating Room Equipment (CORE) 2 Console
- Applicant
- Stryker Instruments MI · US
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2025-03-21
- Date received
- 2024-12-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K243958.pdf
Official FDA record: K243958
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.