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VERTE-STACK® Spinal System 6240486

by Medtronic Sofamor Danek, Inc. 2 variants

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 Number00763000856809 UDI-DIDate5 Apr 2026ListedStatusListed 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  • Withdrawn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
VERTE-STACK® Spinal System
Generic Name
Vertebral body prosthesis
Model / Reference
6240486
Primary DI / UDI-DI
00763000856809
510(k) Number
FDA Product Code
MQP
GMDN Term
Vertebral body prosthesis
Device Class
Class II
Regulation Number
888.3060
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K070173)

Show all (12)

Other devices from Medtronic Sofamor Danek, Inc.

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Properties

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

Other properties (9)

  • 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