meddevicedb.com FDA Device Reference

BIOMARC FIDUCIAL MARKER

K132708 Class II Traditional
Decision Date
2013-12-20
Sponsor / Applicant
Carbon Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K132708
Product Code NEU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2013-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOMARC FIDUCIAL MARKER received FDA 510(k) clearance under submission number K132708, sponsored by Carbon Medical Technologies, 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 2013-12-20.

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.