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JAZZ System JAZZ Evo – 6.35mm Connector Kit

by Implanet

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03607503502627 UDI-DI Date26 Sep 2019ListedStatusListed 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  • Withdrawn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
JAZZ System
Generic Name
Trans-facet-screw internal spinal fixation system, sterile
Model / Ref / Catalog
JAZZ Evo – 6.35mm Connector Kit, 350262
Primary DI / UDI-DI
03607503502627
FDA Product Code
OWI
GMDN Term
Trans-facet-screw internal spinal fixation system, sterile
Device Class
Class II
Regulation Number
888.3010
GUDID distribution status
In Commercial Distribution

Related devices

Category: Trans-facet-screw internal spinal fixation system, sterile

Other devices from Implanet

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Properties

  • Sterile
  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

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