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BIOPSY SCIENCES LLC HYDROMARK BREAST BIOPSY SITE MARKER

K130537 Class II Special
Decision Date
2013-03-29
Sponsor / Applicant
Biopsy Sciences, LLC

Technical Specification

510(k) Submission ID K130537
Product Code NEU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2013-03-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOPSY SCIENCES LLC HYDROMARK BREAST BIOPSY SITE MARKER received FDA 510(k) clearance under submission number K130537, sponsored by Biopsy Sciences, LLC. 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 2013-03-29.

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.