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Na 00-2359-016-38

by Zimmer, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

22 ongoing

This device is named in the recall

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 Number00889024057524 UDI-DI Date5 Dec 2017ListedStatusListed GUDID: in commercial distribution

Recalls

24 recalls · 22 ongoing · FDA

  • 21 recalls, same reason

    • Ongoing Z-1718-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1713-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1725-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1709-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1716-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1727-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1717-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1724-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1720-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1728-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1711-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1714-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1715-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1723-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1721-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1722-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1726-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1719-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1729-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1710-2024 FDA Class II initiated 20 Mar 2024
    • Ongoing Z-1712-2024 FDA Class II initiated 20 Mar 2024

    Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

    • Ongoing Z-2254-2023 FDA Class II initiated 27 Jun 2023

    Thread form issue of the locking holes in that the locking screws would not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock.

  • 2 recalls, same reason

    • Terminated Z-0317-2020 FDA Class II initiated 10 Oct 2019
    • Terminated Z-0310-2020 FDA Class II initiated 10 Oct 2019

    Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Coverage

1 jurisdiction

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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Orthopaedic bone screw (non-sliding)
Model / Ref / Catalog
00-2359-016-38
Primary DI / UDI-DI
00889024057524
510(k) Number
FDA Product Code
HRS, HWC
GMDN Term
Orthopaedic bone screw (non-sliding)
Device Class
Class II
Regulation Number
888.3030, 888.3040
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Length — 16 Millimeter

Related devices

Category: Orthopaedic bone screw (non-sliding)

Cleared under the same submission (K070906)

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Cleared under the same submission (K141734)

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Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

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