# K905655: Nonabsorbable Polypropylene Surgical Mesh

- Pathway: 510(k) (Traditional)
- Applicant: United States Surgical, A Division of Tyco Healthc
- Decided: Dec 31, 1990 after 13 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.
30 later devices descend from it; 4 cite it directly.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K041632: Minimesh Polypropylene Mesh (2004), 27 descendants of its own
- K053361: Modification to: Minimesh Polypropylene Mesh (2006), 16 descendants of its own
- K092207: Restorelle Polypropylene Mesh (2009), 13 descendants of its own
- K090739: Bard Sacrocolpopexy Graft (2009), 9 descendants of its own
- K101722: Alyte Y-Mesh Graft (2011), 8 descendants of its own

Source page: https://510kreport.com/device/K905655
Methodology: https://510kreport.com/methodology