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Ascendant 05-090-10-1406

by Choicespine, LP

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 Number10885862260475 UDI-DI Date16 Nov 2015ListedStatusListed 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  • Withdrawn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
Ascendant
Generic Name
Polymeric spinal fusion cage, sterile
Model / Ref / Catalog
05-090-10-1406
Primary DI / UDI-DI
10885862260475
FDA Product Code
ODP
GMDN Term
Polymeric spinal fusion cage, sterile
Device Class
Class II
Regulation Number
888.3080
GUDID distribution status
In Commercial Distribution
Size
Length — 12 Millimeter
Width — 14 Millimeter
Height — 6 Millimeter

Related devices

Category: Polymeric spinal fusion cage, sterile

Other devices from Choicespine, LP

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Serial Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Manufacturing Date: No