meddevicedb.com FDA Device Reference

UltraCor Twirl Breast Tissue Marker

K152510 Class II Traditional
Decision Date
2016-05-13
Sponsor / Applicant
Bard Peripheral Vascular, Inc.

Technical Specification

510(k) Submission ID K152510
Product Code NEU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2016-05-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UltraCor Twirl Breast Tissue Marker received FDA 510(k) clearance under submission number K152510, sponsored by Bard Peripheral Vascular, 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 2016-05-13.

Classification & Regulation

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