K233800
- 510(k) number
- K233800
- Device name
- Vertos mild Device Kit (MDK-0002)
- Applicant
- Vertos Medical, Inc. CA · US
- Product code
- HRX — Arthroscope
- Decision date
- 2024-05-06
- Date received
- 2023-11-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K233800.pdf
Official FDA record: K233800
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.