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Buck 71279420

by Smith & Nephew, Inc.

Buck 71279420 is a Class II device made by Smith & Nephew, Inc., cleared under FDA 510(k) K211176 on 1 Jul 2022 (1 earlier submission) and listed in FDA GUDID since 29 Aug 2015 (UDI-DI 03596010191076), active as of 23 Oct 2026.

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

Recall on shared 510(k) K211176; other models may be affected

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k) from GUDID NumberK211176 Date1 Jul 2022IssuedStatusActive
United StatesGUDID listing Number03596010191076 UDI-DI Date29 Aug 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • FDA 510(k) K211176 decided 1 Jul 2022 Active· +1 more in the status table
  • FDA GUDID UDI-DI 03596010191076 listed 29 Aug 2015 Listed

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-0326-2025 FDA Class II initiated 15 Oct 2024 on shared 510(k) K211176

    The Bipolar assembly contains an oversized Retainer Ring.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Timeline

4 dated events

  1. Cleared FDA 510(k) K791125
  2. Listed FDA GUDID 03596010191076
  3. Cleared FDA 510(k) K211176
  4. Recall initiated FDA recalls Z-0326-2025

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Buck
Generic name
Polymer orthopaedic cement restrictor, non-bioabsorbable
Model / Ref / Catalog
71279420
Primary DI / UDI-DI
03596010191076
510(k) Number
FDA product code
LZN
GMDN term
Polymer orthopaedic cement restrictor, non-bioabsorbable
Device class
Class II
Regulation number
878.3300
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Polymer orthopaedic cement restrictor, non-bioabsorbable

Cleared under the same submission (K211176)

and 8 more cleared under K211176

Cleared under the same submission (K791125)

and 8 more cleared under K791125

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)