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MODIFICATION TO COALESCENT SURGICAL U-CLIP AND ACCESSORIES

K031623 Class II Special
Decision Date
2003-07-03
Sponsor / Applicant
Coalescent Surgical

Technical Specification

510(k) Submission ID K031623
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2003-07-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO COALESCENT SURGICAL U-CLIP AND ACCESSORIES received FDA 510(k) clearance under submission number K031623, sponsored by Coalescent Surgical. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2003-07-03.

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.