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Autobahn

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
AUTOBAHN FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
AUTOBAHN EVO Retrograde Femoral Nail, 11x440mm, 5°, Ti FDA UDI
Model / Reference
1257.5144S FDA UDI
Description
AUTOBAHN EVO Retrograde Femoral Nail, 11x440mm, 5°, Ti FDA UDI

Identifiers

Primary DI / UDI-DI
00193982498825 FDA UDI
510(k) Number
K220659 FDA UDI
FDA Product Code
HSB FDA UDI
JDS FDA UDI
HWC FDA UDI
GMDN Term
Arthrodesis intramedullary nail, non-distracting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
888.3030 FDA UDI
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

Autobahn by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthrodesis intramedullary nail, non-distracting.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e11e570b-d35e-41e9-a362-7e8d73028ae9 34 fields · synced Jun 6, 2026