meddevicedb.com FDA Device Reference

MICRO STAMPING LIGATING CLIP

K013264 Class II Traditional
Decision Date
2001-11-29
Sponsor / Applicant
Micro Stamping Corp.

Technical Specification

510(k) Submission ID K013264
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2001-11-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO STAMPING LIGATING CLIP received FDA 510(k) clearance under submission number K013264, sponsored by Micro Stamping Corp.. 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 2001-11-29.

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.