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MotionLoc™ NCB® 02.02161.032

by Zimmer, Inc.

Ref 02.02161.032

MotionLoc™ NCB® 02.02161.032 is a device classified as Class IIb in the EU and Class II in the US made by Zimmer, Inc., registered in EUDAMED on 31 Oct 2026 (Basic UDI-DI B-00889024082663), cleared under FDA 510(k) K123918 on 14 Feb 2013 (1 earlier submission) and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 00889024082663), 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) K123918

+1 more

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00889024082663 Basic UDI-DI 00889024082663UDI-DIDate31 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024082663 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK123918 Date14 Feb 2013DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-00889024082663 registered 31 Oct 2026 Active
  • FDA 510(k) K123918 decided 14 Feb 2013 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00889024082663 listed 24 Sep 2015 Listed

Timeline

4 dated events

  1. Cleared FDA 510(k) K101696
  2. Cleared FDA 510(k) K123918
  3. Listed FDA GUDID 00889024082663
  4. Registered EUDAMED B-00889024082663

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  • Withdrawn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
MotionLoc™ NCB®
Generic name
Orthopaedic bone screw (non-sliding)
Model / Ref / Catalog
02.02161.032
Primary DI / UDI-DI
00889024082663
Basic UDI-DI
B-00889024082663
510(k) Number
FDA product code
HWC, HRS
EMDN code
P09120601 Cortical screws
GMDN term
Orthopaedic bone screw (non-sliding)
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3040, 888.3030
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Length — 32 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 screw, non-bioabsorbable, sterile

Cleared under the same submission (K101696)

and 8 more cleared under K101696

Cleared under the same submission (K123918)

and 8 more cleared under K123918

Similar devices in this category

Other devices filed under CORTICAL SCREWS.

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)