meddevicedb.com FDA Device Reference

BACK-TEK

K101227 Class II Traditional
Decision Date
2010-06-23
Sponsor / Applicant
York Biomedical, Inc.

Technical Specification

510(k) Submission ID K101227
Product Code ILY
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2010-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACK-TEK received FDA 510(k) clearance under submission number K101227, sponsored by York Biomedical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2010-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code ILY and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.