meddevicedb.com FDA Device Reference

SIGNIFY BIOACTIVE

K130977 Class II Traditional
Decision Date
2013-12-24
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K130977
Product Code MQV
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3045
Decision Date 2013-12-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIGNIFY BIOACTIVE received FDA 510(k) clearance under submission number K130977, 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 2013-12-24.

Classification & Regulation

This clearance is catalogued under FDA product code MQV and 21 CFR 888.3045, within the Orthopedic review panel as a Class II device.