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ALEUTIAN® Interbody Systems SP-2115-09

by VB Spine LLC

Listed FDA GUDID listing, not in commercial distribution

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 Number10888857308039 UDI-DI Date2 Dec 2016ListedStatusListed GUDID: not 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  • Withdrawn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
ALEUTIAN® Interbody Systems
Generic Name
General internal orthopaedic fixation system implantation kit
Model / Ref / Catalog
SP-2115-09
Primary DI / UDI-DI
10888857308039
FDA Product Code
MQP, MAX, ODP
GMDN Term
General internal orthopaedic fixation system implantation kit
Device Class
Class II
Regulation Number
888.3060, 888.3080
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Width — 18 Millimeter
Length — 45 Millimeter
Height — 14 Millimeter

Other devices from VB Spine LLC

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • 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