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JAZZ System JAZZ Claw – Pre-bent Rod Dia. 4/5.5 L70

by Implanet 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number10889981188221 UDI-DI Date14 Sep 2020ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

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  • Withdrawn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 Claw – Pre-bent Rod Dia. 4/5.5 L70, 360717
Primary DI / UDI-DI
10889981188221
510(k) Number
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

Cleared under the same submission (K191217)

Show all (12)

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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