K233675
- 510(k) number
- K233675
- Device name
- FMS VUE Fluid Management and Tissue Debridement System
- Applicant
- DePuy Mitek, Inc. MA · US
- Product code
- HRX — Arthroscope
- Decision date
- 2024-02-26
- Date received
- 2023-11-16
- 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: K233675.pdf
Official FDA record: K233675
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.