meddevicedb.com FDA Device Reference

TIGER SPINE SYSTEM

K120696 Class II Special
Decision Date
2012-04-02
Sponsor / Applicant
Corelink, LLC

Technical Specification

510(k) Submission ID K120696
Product Code MNI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2012-04-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TIGER SPINE SYSTEM received FDA 510(k) clearance under submission number K120696, sponsored by Corelink, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code MNI and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.