# K222783: MD Mattress Suture Placement Device

- Pathway: 510(k) (Traditional)
- Applicant: Lsi Solutions, Inc.
- Decided: Jan 12, 2024 after 484 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K933887 (1993). 15 ancestors in all.
No later device cites it as a predicate yet.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100593: Suture Placement Device and Accessories, Flexible Suture Placement Device and Accessories, Lsi R Series Suture Placeme, Lsi Solutions, Inc. (2010) Summary page 5.

## Indications for use
The MD™ MATTRESS Suture Placement Device is indicated for use in the approximation of soft tissue and prosthetic materials.

Source page: https://510kreport.com/device/K222783
Methodology: https://510kreport.com/methodology