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Expedium 179778600

by Depuy Spine, Inc.

Expedium 179778600 is a Class II device made by Depuy Spine, Inc., cleared under FDA 510(k) K111136 on 14 Jun 2012 (1 earlier submission) and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 10705034393124), active as of 23 Oct 2026. One FDA recall is linked to it.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10705034393124 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESU from GUDID Traditional NumberK111136 Date14 Jun 2012DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K111136 decided 14 Jun 2012 Active· +1 more in the status table
  • FDA GUDID UDI-DI 10705034393124 listed 24 Sep 2015 Listed

Recalls

1 recall · FDA

    • Terminated Z-1674-2015 FDA Class II initiated 21 Apr 2015

    Device does not mate as intended.

Timeline

4 dated events

  1. Cleared FDA 510(k) K082942
  2. Cleared FDA 510(k) K111136
  3. Recall initiated FDA recalls Z-1674-2015
  4. Listed FDA GUDID 10705034393124

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Expedium
Generic name
Bone-screw internal spinal fixation system rod
Model / Ref / Catalog
179778600
Primary DI / UDI-DI
10705034393124
510(k) Number
FDA product code
OSH, MNH, KWQ, NKB, MNI, KWP
GMDN term
Bone-screw internal spinal fixation system rod
Device class
Class II
Regulation number
888.3070, 888.3060, 888.3050
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone-screw internal spinal fixation system rod

Cleared under the same submission (K082942)

Cleared under the same submission (K111136)

and 8 more cleared under K111136

Similar devices

Other devices filed under FDA product code OSH (Pedicle screw spinal system, adolescent idiopathic scoliosis).

Other devices from Depuy Spine, Inc.

See all devices from Depuy Spine, Inc. →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (10, all answered No)