Skip to content

802503606

by Zimmer, Inc.

Ref 802503606

802503606 is a device classified as Class IIa in the EU and Class II in the US made by Zimmer, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00889024499539), cleared under FDA 510(k) K183457 on 5 Nov 2019 and listed in FDA GUDID since 19 Mar 2020 (UDI-DI 00889024499539), 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) K183457

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-00889024499539 Basic UDI-DI 00889024499539UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024499539 UDI-DI Date19 Mar 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK183457 Date5 Nov 2019DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-00889024499539 registered 29 Oct 2026 Active
  • FDA 510(k) K183457 decided 5 Nov 2019 Active
  • FDA GUDID UDI-DI 00889024499539 listed 19 Mar 2020 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K183457
  2. Listed FDA GUDID 00889024499539
  3. Registered EUDAMED B-00889024499539

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  • Withdrawn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

Generic name
Femoral head prosthesis trial
Device name
HP Heads ZB 12/14 Freedom Head Provisional Instruments
Model / Ref / Catalog
802503606
Primary DI / UDI-DI
00889024499539
Basic UDI-DI
B-00889024499539
510(k) Number
FDA product code
KWZ, OQG, KWY, LPH
EMDN code
L091104 Orthopaedic prostheses positioners, reusable
GMDN term
Femoral head prosthesis trial
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
888.3310, 888.3358, 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 IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa 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: Femoral head prosthesis trial

Cleared under the same submission (K183457)

and 8 more cleared under K183457

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE.

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
Other properties (22, all answered No)