meddevicedb.com FDA Device Reference

PATRIOT TRANSCONTINENTAL M SPACERS

K102313 Class II Traditional
Decision Date
2010-12-03
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K102313
Product Code MAX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2010-12-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATRIOT TRANSCONTINENTAL M SPACERS received FDA 510(k) clearance under submission number K102313, sponsored by Globus Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2010-12-03.

Classification & Regulation

This clearance is catalogued under FDA product code MAX and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.