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Autobahn 1183.1431S

by Globus Medical, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889095734591 UDI-DI Date28 Jun 2019ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Autobahn
Generic Name
Arthrodesis intramedullary nail, non-distracting
Model / Reference
1183.1431S
Primary DI / UDI-DI
00889095734591
510(k) Number
FDA Product Code
JDS, HWC, HSB
GMDN Term
Arthrodesis intramedullary nail, non-distracting
Device Class
Class II
Regulation Number
888.3030, 888.3040, 888.3020
GUDID distribution status
In Commercial Distribution
Size
Length — 315 Millimeter
Outer Diameter — 14 Millimeter

Related devices

Category: Arthrodesis intramedullary nail, non-distracting

Cleared under the same submission (K171108)

Show all (12)

Other devices from Globus Medical, Inc.

See all devices from Globus Medical, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No