K241361
- 510(k) number
- K241361
- Device name
- Arthrex Synergy Vision Endoscopic Imaging System
- Applicant
- Arthrex, Inc. FL · US
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2024-07-25
- Date received
- 2024-05-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K241361.pdf
Official FDA record: K241361
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.