meddevicedb.com FDA Device Reference

AJUST HELICAL ADJUSTABLE SINGLE-INCISION SLING

K123179 Class II Special
Decision Date
2012-11-02
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K123179
Product Code PAH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2012-11-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AJUST HELICAL ADJUSTABLE SINGLE-INCISION SLING received FDA 510(k) clearance under submission number K123179, sponsored by C.R. Bard, Inc.. 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 2012-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code PAH and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.