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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
K191358
05/21/2019
Trident II Acetabular System
Howmedica Osteonics Corp. aka Stryker Orthopaedics
K161569
06/07/2016
Trident« II Tritanium« Acetabular Shells and 6.5 mm Low Profile Hex Screws
Howmedica Osteonics Corp. aka Stryker Orthopaedics
K171768
06/14/2017
Trident« II Acetabular System
Howmedica Osteonics Corp. aka Stryker Orthopaedics
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