# K083039: Veritas Collagen Matrix (Dry)

- Pathway: 510(k) (Traditional)
- Applicant: Synovis Surgical Innovations
- Decided: Nov 26, 2008 after 43 days
- Product code: FTM (Mesh, Surgical)
- 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: 9 generations back to K842066 (1985). 45 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 48 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041669: Veritas Dry Collagen Matrix, Veritas Dry or Veritas PSD, Synovis Surgical Innovations (2004) Summary page 1.
- K062915: Veritas Collagen Matrix, Synovis Surgical Innovations (2006) Summary page 1.

## Most influential descendants
- K192615: Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG) (2019), 1 descendant of its own
- K213125: PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology (2021), 0 descendants of its own

## Indications for use
Veritas Collagen Matrix (Dry) is intended for use as a prosthesis for the surgical repair of soft tissue deficiencies using surgical staplers when staple line reinforcement is needed. Veritas Collagen Matrix (Dry) can be used for reinforcement of staple lines during lung and bronchus resection, during gastric, bariatric, small bowel, mesentery, colon and colorectal procedures, and cardiac surgery (for example, occlusion of the left atrial appendage during open chest procedures. Veritas Collagen Matrix (Dry) minimizes tissue attachment to the device in case of direct contact with viscera.

Source page: https://510kreport.com/device/K083039
Methodology: https://510kreport.com/methodology