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Expedium Spine System

by Medos International SARL 909 variants

Ref 179798060S, 179912540S, 179712955S, 179912860S, 179702550S, 179732535, 179772035, 179771655S, 179971655S, 179712780S, 179712895S, 179912845S, 179702740S, 179732545S, 179712790S, 179963450S, 179712151S, 179912525S, 286782510, 179912550S, 179788530S, 179712865S, 179912530S, 186172355S, 179912945S, 179772045, 179702435S, 179788650S, 179712760S, 186132435S, 179712140S, 179732530S, 179702745S, 179940100S, 179771035S, 179772055, 179712065S, 179732525S, 186112025S, 186132635S, 179970055S, 179970045S, 179970085S, 186112435S, 179722445S, 179702735S, 179952038S, 179952036S, 179912875S, 179712165S, 179988640SModel EXPEDIUM Spine System Connector, EXPEDIUM Spine System Bone Screw, EXPEDIUM Spine System Rod, Viper Reusable Instruments for Insertion and Extraction, EXPEDIUM Spine System Hook

Active European Union and United States

CE MDR 510(k)

Valid until

Not listed

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) K222473↗

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, FDA 510(k), synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0705034a001596A Basic UDI-DI Date18 Mar 2026RegisteredStatusActive
United StatesFDA 510(k) 510(k) NumberK222473 Date13 Oct 2022IssuedStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

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  • Withdrawn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 · 510(k)

Trade Name
Expedium Spine System
Expedium
Device Name
End to End Dual Connector, Fixed Lateral Connector, Open/Closed Connector, SFX Cross Connector, Side by Side Dual Connector
Polyaxial/Monoaxial/Uniplanar Screws Polyaxial/Uniplanar Extended Tab Screws Alar Bone Screw Cable/Wire Screw Fixed/Polyaxial Bolt
Straight rod, Rod, Commercially Pure Rod, Commercially Pure Rod with Hex Ends, Dual Diameter Rod, Dual Diameter Straight Rod, etc.
Angled/Narrow/Wide Blade Hooks, Extended Body Hooks, Reduced Distance Hooks, Left/Right Angled Hooks, Left/Right Offset Hooks
Model / Reference
EXPEDIUM Spine System Connector, 179798060S, EXPEDIUM Spine System Bone Screw, 179912540S, 179712955S, 179912860S, 179702550S, 179732535, EXPEDIUM Spine System Rod, 179772035, 179771655S, 179971655S, 179712780S, 179712895S, 179912845S, 179702740S, 179732545S, 179712790S, 179963450S, 179712151S, 179912525S, Viper Reusable Instruments for Insertion and Extraction, 286782510, 179912550S, 179788530S, 179712865S, 179912530S, 186172355S, 179912945S, 179772045, 179702435S, 179788650S, 179712760S, 186132435S, 179712140S, 179732530S, 179702745S, 179940100S, 179771035S, 179772055, 179712065S, 179732525S, 186112025S, 186132635S, 179970055S, 179970045S, 179970085S, 186112435S, 179722445S, 179702735S, EXPEDIUM Spine System Hook, 179952038S, 179952036S, 179912875S, 179712165S, 179988640S
Primary DI / UDI-DI
10705034385396, 10705034386317, 10705034383811, 10705034386751, 10705034265223, 10705034073682, 10705034077888, 10705034384801, 10705034393346, 10705034267180, 10705034605234, 10705034386720, 10705034265315, 10705034268989, 10705034383651, 10705034393155, 10705034605524, 10705034386287, 10705034215242, 10705034386331, 10705034270463, 10705034383736, 10705034386294, 10705034406190, 10705034386881, 10705034077901, 10705034265131, 10705034385204, 10705034383613, 10705034404950, 10705034383378, 10705034268927, 10705034265322, 10705034387390, 10705034384764, 10705034077925, 10705034383316, 10705034268910, 10705034404134, 10705034405131, 10705034393223, 10705034393209, 10705034393285, 10705034404257, 10705034268545, 10705034265308, 10705034387628, 10705034387611, 10705034386782, 10705034383392, 10705034393667
Basic UDI-DI
0705034a001596A, 0705034a0015766, 0705034a0016667, 0705034a001365W, 0705034a001615V
EMDN Code
P09070302, L091001
Device Class
Class IIb
Class I
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
CH-MF-000014268
Authorised representative
DePuy Ireland UC IE-AR-000009328

Other devices from Medos International SARL

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Properties

  • Sterile YesEUDAMEDNoEUDAMED
  • Implantable YesEUDAMEDNoEUDAMED
  • Reusable NoEUDAMEDYesEUDAMED
  • Sutures

Other properties (10)

  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No