K241250
- 510(k) number
- K241250
- Device name
- 3DMax Light Mesh
- Applicant
- Davol Inc., Subsidiary of C. R. Bard, Inc. RI · US
- Product code
- FTL — Mesh, Surgical, Polymeric
- Decision date
- 2024-06-14
- Date received
- 2024-05-03
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.0 MB · U.S. public domain
Also available from FDA: K241250.pdf
Official FDA record: K241250
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.