meddevicedb.com FDA Device Reference

EMBRACE THERMOPLASTIC

K120335 Class II Traditional
Decision Date
2012-05-03
Sponsor / Applicant
Bionix Development Corp.

Technical Specification

510(k) Submission ID K120335
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2012-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMBRACE THERMOPLASTIC received FDA 510(k) clearance under submission number K120335, sponsored by Bionix Development Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-05-03.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.