meddevicedb.com FDA Device Reference

AUTOBAHN(R) EVO Femoral Nails

K220659 Class II Traditional
Decision Date
2022-09-09
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K220659
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2022-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTOBAHN(R) EVO Femoral Nails received FDA 510(k) clearance under submission number K220659, 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 2022-09-09.

Classification & Regulation

This clearance is catalogued under FDA product code HSB and 21 CFR 888.3020, within the Orthopedic review panel as a Class II device.