meddevicedb.com FDA Device Reference

SURGICAL TISSUE MANAGEMENT SYSTEM

K111202 Class II Traditional
Decision Date
2012-01-20
Sponsor / Applicant
Olympus Medical Systems Corp.

Technical Specification

510(k) Submission ID K111202
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2012-01-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL TISSUE MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K111202, sponsored by Olympus Medical Systems Corp.. 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 2012-01-20.

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.