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EVEREST® Spinal System ME5112-01040

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 Number10888857324879 UDI-DI Date15 Dec 2016ListedStatusListed 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  • Withdrawn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
EVEREST® Spinal System
Generic Name
Spinal bone screw, non-bioabsorbable
Model / Ref / Catalog
ME5112-01040
Description
Sacroiliac Screw Extended Tab Cannulated Size Ø10.5x40 mm
Primary DI / UDI-DI
10888857324879
FDA Product Code
KWQ, NKB, MNI, MNH, KWP, OSH
GMDN Term
Spinal bone screw, non-bioabsorbable
Device Class
Class II
Regulation Number
888.3060, 888.3070, 888.3050
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 10.5 Millimeter
Length — 40 Millimeter

Related devices

Category: Spinal bone screw, non-bioabsorbable

Other devices from VB Spine LLC

See all devices from VB Spine LLC →

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