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MILTEX LIGATING CLIP

K052018 Class II Traditional
Decision Date
2005-11-04
Sponsor / Applicant
Miltex, Inc.

Technical Specification

510(k) Submission ID K052018
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2005-11-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILTEX LIGATING CLIP received FDA 510(k) clearance under submission number K052018, sponsored by Miltex, Inc.. 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 2005-11-04.

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.