# K241250: 3DMax Light Mesh

- Pathway: 510(k) (Special)
- Applicant: Davol Inc., Subsidiary of C. R. Bard, Inc.
- Decided: Jun 14, 2024 after 42 days
- Product code: FTL (Mesh, Surgical, Polymeric)
- Device class: 2
- Regulation: 21 CFR 878.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s summary for it could not be read, so its predicates are not known.

Source page: https://510kreport.com/device/K241250
Methodology: https://510kreport.com/methodology