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60-23124

by Stryker Corp.

Part of a family of 48 devices: see the family page

Ref 60-23124Model 08858251003082SM

60-23124 is a device classified as Class IIa in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 24 Sep 2026 (Basic UDI-DI 08858251003082SM), cleared under FDA 510(k) K070876 on 27 Apr 2007 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 04546540247322), active as of 24 Oct 2026.

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

CE MDR 510(k)

Valid until

No date given

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

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K070876

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251003082SM Basic UDI-DI 04546540247322UDI-DIDate24 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04546540247322 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK070876 Date27 Apr 2007DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 08858251003082SM registered 24 Sep 2026 Active
  • FDA 510(k) K070876 decided 27 Apr 2007 Active
  • FDA GUDID UDI-DI 04546540247322 listed 24 Sep 2016 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K070876
  2. Listed FDA GUDID 04546540247322
  3. Registered EUDAMED 08858251003082SM

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
VariAx
Generic name
Fluted surgical drill bit, single-use
Device name
Variax Instruments - Drilling Instrumentation - Class Iia - Non Sterile
Model / Ref / Catalog
60-23124, 08858251003082SM
Primary DI / UDI-DI
04546540247322
Basic UDI-DI
08858251003082SM
510(k) Number
FDA product code
HBE
EMDN code
P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
GMDN term
Fluted surgical drill bit, single-use
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
882.4310
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 27.0 Millimeter
Length — 141.0 Millimeter

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: Fluted surgical drill bit, single-use

Cleared under the same submission (K070876)

and 8 more cleared under K070876

Similar devices in this category

Other devices filed under OSTEOSYNTHESIS DEVICES, DEVICES FOR TENDON AND LIGAMENT SYNTHESIS - ACCESSORIES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Single use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Lot / batch number
Other properties (20, all answered No)