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Autobahn

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name
AUTOBAHN FDA UDI
Generic Name
Implantable bone washer FDA UDI
Device Name
AUTOBAHN EVO Retrograde Femoral Nail Washer for Nut, Ti FDA UDI
Model / Reference
1257.0420 FDA UDI
Description
AUTOBAHN EVO Retrograde Femoral Nail Washer for Nut, Ti FDA UDI

Identifiers

Primary DI / UDI-DI
00193982471224 FDA UDI
510(k) Number
K220659 FDA UDI
FDA Product Code
HSB FDA UDI
HWC FDA UDI
JDS FDA UDI
GMDN Term
Implantable bone washer FDA UDI

Classification

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

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Implantable bone washer

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

Similar devices

Also classified as Implantable bone washer.

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 0c53a8ba-03a4-4ca0-85c3-87627b99de66 34 fields · synced Jun 6, 2026