meddevicedb.com FDA Device Reference

SOLID CLIP™ Single Use Clip Applier

K221495 Class II Traditional
Decision Date
2024-07-18
Sponsor / Applicant
Medscope Biotech Co., Ltd.

Technical Specification

510(k) Submission ID K221495
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2024-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOLID CLIP™ Single Use Clip Applier received FDA 510(k) clearance under submission number K221495, sponsored by Medscope Biotech Co., 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 2024-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code FZP and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.