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ALEUTIAN® Interbody Systems SP-4214-12

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 Number10888857521360 UDI-DI Date26 Apr 2021ListedStatusListed 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  • Withdrawn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
ALEUTIAN® Interbody Systems
Generic Name
General internal orthopaedic fixation system implantation kit
Model / Ref / Catalog
SP-4214-12
Primary DI / UDI-DI
10888857521360
FDA Product Code
ODP, MAX, MQP
GMDN Term
General internal orthopaedic fixation system implantation kit
Device Class
Class II
Regulation Number
888.3080, 888.3060
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Height — 5 Millimeter
Angle — 7 degree
Width — 12 Millimeter
Depth — 14 Millimeter

Related devices

Category: General internal orthopaedic fixation system implantation kit

Other devices from VB Spine LLC

See all devices from VB Spine LLC →

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