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ExcelsiusHub

K211616 Class II Traditional
Decision Date
2021-08-25
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K211616
Product Code OLO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2021-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ExcelsiusHub received FDA 510(k) clearance under submission number K211616, sponsored by Globus Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2021-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.