meddevicedb.com FDA Device Reference

PIXEL 3 SYSTEM

DEN130015 Class II Direct
Decision Date
2014-05-09
Sponsor / Applicant
Gauss Surgical, Inc.,

Technical Specification

510(k) Submission ID DEN130015
Product Code PBZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2750
Decision Date 2014-05-09
Clearance Pathway Direct

Official Documentation

No FDA summary/statement PDF is linked for this clearance in the current dataset. Consult the product code and regulation citation above to locate predicate documentation.

Clearance Summary

PIXEL 3 SYSTEM received FDA 510(k) clearance under submission number DEN130015, sponsored by Gauss Surgical, Inc.,. The device was reviewed via the Direct premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2014-05-09.

Classification & Regulation

This clearance is catalogued under FDA product code PBZ and 21 CFR 880.2750, within the General Hospital review panel as a Class II device.