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TISSUE SITE MARKING SYSTEM

K062528 Class II Traditional
Decision Date
2007-01-26
Sponsor / Applicant
Suros Surgical Systems, Inc.

Technical Specification

510(k) Submission ID K062528
Product Code NEU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2007-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TISSUE SITE MARKING SYSTEM received FDA 510(k) clearance under submission number K062528, sponsored by Suros Surgical Systems, 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 2007-01-26.

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.