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MODIFICATION TO BIOMARC TISSUE MARKER

K063193 Class II Special
Decision Date
2006-11-21
Sponsor / Applicant
Carbon Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K063193
Product Code NEU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2006-11-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO BIOMARC TISSUE MARKER received FDA 510(k) clearance under submission number K063193, sponsored by Carbon Medical Technologies, Inc.. 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 2006-11-21.

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.