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CHESAPEAKE® Stabilization System 2013-22040L15

by VB Spine LLC

CHESAPEAKE® Stabilization System 2013-22040L15 is a Class II device made by VB Spine LLC, listed in FDA GUDID since 27 Nov 2018 (UDI-DI 10888857028494), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10888857028494 UDI-DI Date27 Nov 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
CHESAPEAKE® Stabilization System
Generic name
Vertebral body prosthesis
Model / Ref / Catalog
2013-22040L15
Primary DI / UDI-DI
10888857028494
FDA product code
OVD
GMDN term
Vertebral body prosthesis
Device class
Class II
Regulation number
888.3080
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 30 Millimeter
Width — 40 Millimeter
Angle — 15 degree
Height — 20 Millimeter

Related devices

Category: Vertebral body prosthesis

Other devices from VB Spine LLC

See all devices from VB Spine LLC →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (10, all answered No)