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Xmcp 102-40020

by Extremity Medical, LLC

Ref 102-40020

Xmcp 102-40020 is a device classified as Class IIb in the EU and Class II in the US made by Extremity Medical, LLC, registered in EUDAMED on 19 Aug 2026 (Basic UDI-DI B-00842078101933), cleared under FDA 510(k) K121417 on 18 Jul 2012 and listed in FDA GUDID since 27 Jun 2019 (UDI-DI 00842078101933), active as of 24 Oct 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 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K121417

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/MDD EUDAMED NumberB-00842078101933 Basic UDI-DI 00842078101933UDI-DIDate19 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00842078101933 UDI-DI Date27 Jun 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Special NumberK121417 Date18 Jul 2012DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-00842078101933 registered 19 Aug 2026 Active
  • FDA 510(k) K121417 decided 18 Jul 2012 Active
  • FDA GUDID UDI-DI 00842078101933 listed 27 Jun 2019 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K121417
  2. Listed FDA GUDID 00842078101933
  3. Registered EUDAMED B-00842078101933

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  • Withdrawn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
Xmcp
Generic name
Orthopaedic bone screw, non-bioabsorbable, non-sterile
Model / reference
102-40020
Primary DI / UDI-DI
00842078101933
Basic UDI-DI
B-00842078101933
510(k) Number
FDA product code
HWC
EMDN code
P09120603 Cannulated screws
GMDN term
Orthopaedic bone screw, non-bioabsorbable, non-sterile
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3040
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

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, non-sterile

Cleared under the same submission (K121417)

and 8 more cleared under K121417

Similar devices in this category

Other devices filed under CANNULATED SCREWS.

Other devices from Extremity Medical, LLC

See all devices from Extremity Medical, LLC →

Properties

  • Sterilise before use
  • Single use
  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Lot / batch number
Other properties (18, all answered No)