meddevicedb.com FDA Device Reference

CM00622 LINC Skin Closure System (CM00622 LINC)

K233460 Class II Traditional
Decision Date
2024-07-15
Sponsor / Applicant
Connexicon Medical , Ltd.

Technical Specification

510(k) Submission ID K233460
Product Code OMD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4011
Decision Date 2024-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CM00622 LINC Skin Closure System (CM00622 LINC) received FDA 510(k) clearance under submission number K233460, sponsored by Connexicon Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-07-15.

Classification & Regulation

This clearance is catalogued under FDA product code OMD and 21 CFR 878.4011, within the General, Plastic Surgery review panel as a Class II device.