K243020
- 510(k) number
- K243020
- Device name
- MIDASVu
- Applicant
- Intravu, Inc. CA · US
- Product code
- HRX — Arthroscope
- Decision date
- 2024-12-02
- Date received
- 2024-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K243020.pdf
Official FDA record: K243020
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.