Skip to content

Barricaid® Narrow Anchor ACD - Reusable Instruments Kit 4001009

by Intrinsic Therapeutics

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

1 closed

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM906KITD7NARROW0 UDI-DI Date15 Jan 2026ListedStatusListed GUDID: in commercial distribution

Recalls

1 recall · FDA

    • Terminated Z-2798-2020 FDA Class II initiated 24 Jul 2020

    The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Barricaid® Narrow Anchor ACD - Reusable Instruments Kit
Generic Name
Intervertebral disc prolapse repair implant
Model / Ref / Catalog
4001009, KIT-D7-NARROW
Primary DI / UDI-DI
M906KITD7NARROW0
PMA Number
FDA Product Code
QES
GMDN Term
Intervertebral disc prolapse repair implant
Device Class
Class III
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Cleared under the same submission (P160050)

Other devices from Intrinsic Therapeutics

See all devices from Intrinsic Therapeutics →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Manufacturing Date: No