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YUKON OCT Spinal System 7611-63545

by VB Spine LLC

YUKON OCT Spinal System 7611-63545 is a Class II device made by VB Spine LLC, listed in FDA GUDID since 25 Aug 2017 (UDI-DI 10888857350885), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10888857350885 UDI-DI Date25 Aug 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  • Withdrawn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
YUKON OCT Spinal System
Generic name
Bone-screw internal spinal fixation system rod
Model / Ref / Catalog
7611-63545
Primary DI / UDI-DI
10888857350885
FDA product code
NKG, KWP
GMDN term
Bone-screw internal spinal fixation system rod
Device class
Class II
Regulation number
888.3075, 888.3050
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Conditional
Size
Length — 45 Millimeter
Outer Diameter — 3.5 Millimeter

Related devices

Category: Bone-screw internal spinal fixation system rod

Other devices from VB Spine LLC

See all devices from VB Spine LLC →

Properties

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