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XtraFix® 00-5214-040-25

by Zimmer, Inc.

Ref 00-5214-040-25

XtraFix® 00-5214-040-25 is a device classified as Class IIb in the EU and Class II in the US made by Zimmer, Inc., registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI B-00889024081475), cleared under FDA 510(k) K131413 on 28 Jan 2014 and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 00889024081475), active as of 7 Nov 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 7 Nov 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K131413

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00889024081475 Basic UDI-DI 00889024081475UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024081475 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK131413 Date28 Jan 2014DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-00889024081475 registered 2 Nov 2026 Active
  • FDA 510(k) K131413 decided 28 Jan 2014 Active
  • FDA GUDID UDI-DI 00889024081475 listed 24 Sep 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K131413
  2. Listed FDA GUDID 00889024081475
  3. Registered EUDAMED B-00889024081475

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
XtraFix®
Generic name
Orthopaedic bone pin, non-bioabsorbable
Device name
Mfx_xtra FIX_PIN_4MM Half 25mm Thd Blt Sml
Model / Ref / Catalog
00-5214-040-25
Primary DI / UDI-DI
00889024081475
Basic UDI-DI
B-00889024081475
510(k) Number
FDA product code
JDW
EMDN code
P09120399 Bone fixation wires - other
GMDN term
Orthopaedic bone pin, non-bioabsorbable
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3040
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Conditional
Size
Length — 120 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Orthopaedic bone pin, non-bioabsorbable

Cleared under the same submission (K131413)

and 8 more cleared under K131413

Similar devices in this category

Other devices filed under BONE FIXATION WIRES - OTHER.

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (20, all answered No)