K262406
- 510(k) number
- K262406
- Device name
- EluPro Antibiotic-Eluting BioEnvelope
- Applicant
- Boston Scientific MN · US
- Product code
- FTM — Mesh, Surgical
- Decision date
- 2026-08-12
- Date received
- 2026-07-15
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K262406.pdf
Official FDA record: K262406
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.