meddevicedb.com FDA Device Reference

Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device

K220091 Class II Traditional
Decision Date
2022-08-26
Sponsor / Applicant
Xiros, Ltd.

Technical Specification

510(k) Submission ID K220091
Product Code FTL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2022-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device received FDA 510(k) clearance under submission number K220091, sponsored by Xiros, 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 2022-08-26.

Classification & Regulation

This clearance is catalogued under FDA product code FTL and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.