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ACE MONOPOLAR ATTACHMENT

K123061 Class II Traditional
Decision Date
2013-08-13
Sponsor / Applicant
Bioeconeer, Inc.

Technical Specification

510(k) Submission ID K123061
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2013-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACE MONOPOLAR ATTACHMENT received FDA 510(k) clearance under submission number K123061, sponsored by Bioeconeer, 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 2013-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.