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Sirion GA204010C

by Astura Medical

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 Number00841379192237 UDI-DIDate6 Jul 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  • Withdrawn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
Sirion
Generic Name
Polymeric spinal interbody fusion cage
Model / Ref / Catalog
GA204010C
Primary DI / UDI-DI
00841379192237
FDA Product Code
KWQ, MAX, OVD
GMDN Term
Polymeric spinal interbody fusion cage
Device Class
Class II
Regulation Number
888.3060, 888.3080
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Angle — 12 degree
Length — 40 Millimeter
Width — 20 Millimeter
Height — 10 Millimeter

Other devices from Astura Medical

See all devices from Astura Medical →

Properties

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

Other properties (10)

  • 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
  • Manufacturing Date: No