meddevicedb.com FDA Device Reference

SMALL STATURE SPACERS

K063393 Class II Traditional
Decision Date
2007-06-25
Sponsor / Applicant
Biomet Spine

Technical Specification

510(k) Submission ID K063393
Product Code MQP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2007-06-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMALL STATURE SPACERS received FDA 510(k) clearance under submission number K063393, sponsored by Biomet Spine. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-06-25.

Classification & Regulation

This clearance is catalogued under FDA product code MQP and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.