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Avenir Complete® 574777420

by Zimmer, Inc.

Ref 574777420

Avenir Complete® 574777420 is a device classified as Class I in the EU and Class II in the US made by Zimmer, Inc., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00889024509832), cleared under FDA 510(k) K182048 on 7 Dec 2018 and listed in FDA GUDID since 19 Jun 2019 (UDI-DI 00889024509832), 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) K182048

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-00889024509832 Basic UDI-DI 00889024509832UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024509832 UDI-DI Date19 Jun 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK182048 Date7 Dec 2018DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-00889024509832 registered 30 Oct 2026 Active
  • FDA 510(k) K182048 decided 7 Dec 2018 Active
  • FDA GUDID UDI-DI 00889024509832 listed 19 Jun 2019 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K182048
  2. Listed FDA GUDID 00889024509832
  3. Registered EUDAMED B-00889024509832

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  • Withdrawn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
Avenir Complete®
Generic name
Bone awl, reusable
Device name
HP Avenir Complete Starter Awl Instrument
Model / Ref / Catalog
574777420
Primary DI / UDI-DI
00889024509832
Basic UDI-DI
B-00889024509832
510(k) Number
FDA product code
KWZ, LZO, LWJ, MEH, KWY
EMDN code
L090999 Orthopaedic surgery cutting instruments, reusable - other
GMDN term
Bone awl, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
888.3310, 888.3353, 888.3360, 888.3390
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Bone awl, reusable

Cleared under the same submission (K182048)

and 8 more cleared under K182048

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER.

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)