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Avenue T AT0065P

by Ldr Spine USA

Avenue T AT0065P is a Class II device made by Ldr Spine USA, listed in FDA GUDID since 12 Apr 2017 (UDI-DI 03662663001977), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03662663001977 UDI-DI Date12 Apr 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Avenue T
Generic name
Polymeric spinal fusion cage, sterile
Model / Ref / Catalog
AT0065P
Primary DI / UDI-DI
03662663001977
FDA product code
OVD
GMDN term
Polymeric spinal fusion cage, sterile
Device class
Class II
Regulation number
888.3080
GUDID distribution status
In Commercial Distribution
Size
Angle — 9 degree
Length — 34 Millimeter
Height — 16 Millimeter

Related devices

Category: Polymeric spinal fusion cage, sterile

Other devices from Ldr Spine USA

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)