Skip to content

Cook G43200

by Cook Incorporated

Cook G43200 (CVAK-100) is a Class II device made by Cook Incorporated, listed in FDA GUDID since 24 Oct 2015 (UDI-DI 10827002432007), 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 Number10827002432007 UDI-DI Date24 Oct 2015ListedStatusListed 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  • Withdrawn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
Cook
Generic name
Vertebral bone biopsy procedure kit, single-use
Model / Ref / Catalog
G43200, CVAK-100
Primary DI / UDI-DI
10827002432007
FDA product code
NDN
GMDN term
Vertebral bone biopsy procedure kit, single-use
Device class
Class II
Regulation number
888.3027
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NDN (CEMENT, BONE, VERTEBROPLASTY).

Other devices from Cook Incorporated

See all devices from Cook Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Combination product
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)