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Star Tissue Marker

K170905 Class II Special
Decision Date
2017-04-27
Sponsor / Applicant
Scion Medical Technologies, LLC

Technical Specification

510(k) Submission ID K170905
Product Code NEU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2017-04-27
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Star Tissue Marker received FDA 510(k) clearance under submission number K170905, sponsored by Scion Medical Technologies, LLC. 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 2017-04-27.

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.