FDA.reportPublic FDA data

Device Listing 1666280155

Listing Summary#

Listing key
1666280155
Premarket submission
K220838
Device
Artisan Bone Plug, Universal Cement Restrictor
Applicant
Howmedica Osteonics, Dba Stryker Orthopaedics
Product code
LZN
Decision date
2022-05-20