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EleVation Breast Biopsy System

K211933 Class II Special
Decision Date
2021-07-15
Sponsor / Applicant
Bard Peripheral Vascular

Technical Specification

510(k) Submission ID K211933
Product Code KNW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 2021-07-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EleVation Breast Biopsy System received FDA 510(k) clearance under submission number K211933, sponsored by Bard Peripheral Vascular. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2021-07-15.

Classification & Regulation

This clearance is catalogued under FDA product code KNW and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.