K260317
- 510(k) number
- K260317
- Device name
- Artelon Convenience Kits
- Applicant
- International Life Sciences GA · US
- Product code
- QWJ — Mesh, Surgical, Polymeric, Resorbable, Orthopedics,
- Decision date
- 2026-04-09
- Date received
- 2026-01-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K260317.pdf
Official FDA record: K260317
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.