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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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