# K202551: Cor-Knot Micro

- Pathway: 510(k) (Traditional)
- Applicant: Lsi Solutions, Inc.
- Decided: Jun 24, 2021 after 294 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: 2 generations back to K954853 (1995). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981531: Suture Placement Device and Accessories, Lsi Solutions (1998) Summary page 12.

## Indications for use
The COR-KNOT MICRO™ device with COR-KNOT MICRO™ fastener when used in conjunction with USP 6-0, 7-0, or 8-0 polypropylene surgical suture, is indicated for use in the approximation of soft tissue.

Source page: https://510kreport.com/device/K202551
Methodology: https://510kreport.com/methodology