# K150906: ULTRAPRO ADVANCED Macroporous Partically Absorbable Mesh

- Pathway: 510(k) (Traditional)
- Applicant: Ehicon, Inc.
- Decided: Jul 24, 2015 after 112 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
Longest line of descent: 1 generation back to K033337 (2004). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033337: Ultrapro Mesh, ETHICON, Inc. (2004) Summary page 4.

## Most influential descendants
- K180910: ULTRAPRO Mesh and ULTRAPRO ADVANCED (2018), 0 descendants of its own

## Indications for use
ULTRAPRO ADVANCED™ Mesh may be used for the repair of abdominal fascial deficiencies, such as hernias, that require the addition of a reinforcing or bridging material to obtain the desired surgical result.

Source page: https://510kreport.com/device/K150906
Methodology: https://510kreport.com/methodology