FDA 510(k) Applications Submitted by Howmedica Osteonics, dba Stryker Orthopaedics
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220838 | 03/22/2022 | Artisan Bone Plug, Universal Cement Restrictor | Howmedica Osteonics, dba Stryker Orthopaedics |
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