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Suzuka Interbody Fusion System ALR509

by Altus Spine

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 NumberB417ALR5091 UDI-DI Date22 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  • Withdrawn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
Suzuka Interbody Fusion System
Generic Name
Polymeric spinal interbody fusion cage
Model / Reference
ALR509
Description
Interbody Fusion Device, PEEK ALR, 9mm 5 degree
Primary DI / UDI-DI
B417ALR5091
FDA Product Code
MQP
GMDN Term
Polymeric spinal interbody fusion cage
Device Class
Class II
Regulation Number
888.3060
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Height — 9 Millimeter
Width — 14 Millimeter
Angle — 5 degree
Length — 12.5 Millimeter

Related devices

Category: Polymeric spinal interbody fusion cage

Other devices from Altus Spine

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Properties

  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

  • Sterile: 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