AUTOBAHN(R) EVO Femoral Nails

FDA 510(k) K220659 · Globus Medical, Inc.

Substantially Equivalent

510(k) numberK220659

Submission

Device name
AUTOBAHN(R) EVO Femoral Nails
Applicant
Globus Medical, Inc.
Audubon, PA, US
Received
March 7, 2022
Decision date
September 9, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HSB – Rod, Fixation, Intramedullary And Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3020
Specialty
Orthopedic
Implant
Yes

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K252016Arthrex Humeral NailsHSB · Traditional Arthrex, Inc.03/20/2026SE
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Questions and answers

When was AUTOBAHN(R) EVO Femoral Nails cleared by the FDA?

AUTOBAHN(R) EVO Femoral Nails (K220659) received a 510(k) decision of Substantially Equivalent on September 9, 2022, 186 days after the submission was received.

What is the product code of K220659?

The FDA product code is HSB – Rod, Fixation, Intramedullary And Accessories, a Class II (moderate risk) device regulated under 21 CFR 888.3020.