# K192615: Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG)

- Pathway: 510(k) (Traditional)
- Applicant: Synovis Life Technologies, Inc. (Baxter International Inc.)
- Decided: Dec 17, 2019 after 85 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: 10 generations back to K842066 (1985). 46 ancestors in all.
1 later device descends 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 4.
- K083039: Veritas Collagen Matrix (Dry), Synovis Surgical Innovations (2008) Summary page 4.

## Most influential descendants
- K213125: PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology (2021), 0 descendants of its own

## Indications for use
PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology (PSDV-SG) is intended for use as a prosthesis for the surgical repair of soft tissue deficiencies using surgical staplers when staple line reinforcement is needed. PSDV-SG can be used for reinforcement of staple lines during bariatric, gastric, small bowel, colon and colorectal procedures.

Source page: https://510kreport.com/device/K192615
Methodology: https://510kreport.com/methodology