FDA 510(k) Applications Submitted by Howmedica Osteonics Corp. (aka Stryker Orthopaedics)

FDA 510(k) Number Submission Date Device Name Applicant
K190991 04/15/2019 Triathlon Tritanium Central Femoral Cone Augment, Triathlon Femoral Distal Augment Howmedica Osteonics Corp. (aka Stryker Orthopaedics)
K193233 11/25/2019 Restoration« Modular Hip System Howmedica Osteonics Corp. (aka Stryker Orthopaedics)


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