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Fuson Bone Plug, Radiopaque

by Zimmer, Inc.

510(k) K800142

Fuson Bone Plug, Radiopaque is a Class II device made by Zimmer, Inc., cleared under FDA 510(k) K800142 on 19 Feb 1980, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK800142 Date19 Feb 1980ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
JDS
Device class
Class II
Regulation
21 CFR Part 888.3030
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Devices cleared under K800142

4 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K800142
UDI-DISize and differences
1109-11
Zimmer, Inc.
1109-1100889024432918 —On the market
8011-10-01
Zimmer, Inc.
8011-10-0100889024376724 —On the market
8011-20-01
Zimmer, Inc.
8011-20-0100889024376748 —On the market
8011-30-01
Zimmer, Inc.
8011-30-0100889024376755 —On the market

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →