# K213125: PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology

- Pathway: 510(k) (Special)
- Applicant: Synovis Life Technologies. Inc. (A Subsidiary of Baxter
- Decided: Oct 27, 2021 after 30 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: 11 generations back to K842066 (1985). 47 ancestors in all.
No later device cites it as a predicate yet.
0 of 48 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192615: Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG), Synovis Life Technologies, Inc. (Baxter International Inc.) (2019) Summary page 4.

## Indications for use
PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology 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/K213125
Methodology: https://510kreport.com/methodology