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NEXUS LIGATING CLIP

K053255 Class II Traditional
Decision Date
2006-03-14
Sponsor / Applicant
Microsurgical Laboratories,Inc.Dba Wexler Surgical

Technical Specification

510(k) Submission ID K053255
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2006-03-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEXUS LIGATING CLIP received FDA 510(k) clearance under submission number K053255, sponsored by Microsurgical Laboratories,Inc.Dba Wexler Surgical. 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 2006-03-14.

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.