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Anthem 71422923

by Smith & Nephew, Inc.

Anthem 71422923 is a Class II device made by Smith & Nephew, Inc., cleared under FDA 510(k) K230653 on 4 May 2023 (1 earlier submission) and listed in FDA GUDID since 8 Jun 2017 (UDI-DI 00885556655740), active as of 23 Oct 2026. One FDA recall is linked to it.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK230653 Date4 May 2023DecidedStatusActive
United StatesGUDID listing Number00885556655740 UDI-DI Date8 Jun 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • FDA 510(k) K230653 decided 4 May 2023 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00885556655740 listed 8 Jun 2017 Listed

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-2621-2023 FDA Class II initiated 31 Aug 2023

    The firm conducting a recall due to a complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 4N LT implant instead of a LEGION NARROW PSvOXIN SZ 5N LT as described on the product label.

Timeline

4 dated events

  1. Cleared FDA 510(k) K170648
  2. Listed FDA GUDID 00885556655740
  3. Cleared FDA 510(k) K230653
  4. Recall initiated FDA recalls Z-2621-2023

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Anthem
Generic name
Uncoated knee femur prosthesis, metallic
Model / Ref / Catalog
71422923
Primary DI / UDI-DI
00885556655740
510(k) Number
FDA product code
JWH
GMDN term
Uncoated knee femur prosthesis, metallic
Device class
Class II
Regulation number
888.3560
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Uncoated knee femur prosthesis, metallic

Cleared under the same submission (K170648)

and 8 more cleared under K170648

Cleared under the same submission (K230653)

and 8 more cleared under K230653

Similar devices in this category

Other devices filed under Uncoated knee femur prosthesis, metallic.

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)