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CASCADIA™ Interbody System 402-90399

by VB Spine LLC

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

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 Number10888857303386 UDI-DI Date7 Aug 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
CASCADIA™ Interbody System
Generic name
General internal orthopaedic fixation system implantation kit
Model / Ref / Catalog
402-90399
Primary DI / UDI-DI
10888857303386
FDA product code
MAX, ODP
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class II
Regulation number
888.3080
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Height — 11 Millimeter
Length — 13 Millimeter
Width — 16 Millimeter

Related devices

Category: General internal orthopaedic fixation system implantation kit

Other devices from VB Spine LLC

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number

Other properties (12)

  • Supplied sterile: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No