K242009
- 510(k) number
- K242009
- Device name
- 360CAS Knee
- Applicant
- Kico Knee Innovation Company Pty, Ltd. AU
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2024-08-08
- Date received
- 2024-07-10
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K242009.pdf
Official FDA record: K242009
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.