K243008
- 510(k) number
- K243008
- Device name
- Arthrex NanoScope System
- Applicant
- Arthrex, Inc. FL · US
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2025-01-22
- Date received
- 2024-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
510(k) Summary (official FDA PDF): K243008.pdf
Official FDA record: K243008
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.