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Evos 72402420

by Smith & Nephew, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

2 closed

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 Number00885556428092 UDI-DI Date21 Sep 2015ListedStatusListed GUDID: in commercial distribution

Recalls

2 recalls · FDA

    • Terminated Z-2945-2020 FDA Class II initiated 24 Aug 2020

    Multiple or incorrect expiration dates were provided on the affected designation labels.

    • Terminated Z-0408-2018 FDA Class II initiated 29 Nov 2017

    One lot of EVOS 2.4MM Flex Plate 6 Hole packaging contained templates.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Evos
Generic Name
Orthopaedic bone screw (non-sliding)
Model / Ref / Catalog
72402420
Primary DI / UDI-DI
00885556428092
510(k) Number
FDA Product Code
HRS
GMDN Term
Orthopaedic bone screw (non-sliding)
Device Class
Class II
Regulation Number
888.3030
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Orthopaedic bone screw (non-sliding)

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Cleared under the same submission (K210837)

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Cleared under the same submission (K213126)

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Other devices from Smith & Nephew, Inc.

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Properties

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

Other properties (8)

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