Howmedica Osteonics Corp. (Aka Stryker Orthopaedics) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Howmedica Osteonics Corp. (Aka Stryker Orthopaedics) - FDA 510(k) Cle...
Recent clearances: Restoration® Modular Hip System, Triathlon Tritanium Central Femoral Cone Augment, Triathlon Femoral Distal Augment
2
Total
2
Cleared
0
Denied
Howmedica Osteonics Corp. (Aka Stryker Orthopaedics) has 2 FDA 510(k) cleared medical devices. Based in Malwah, US.
Historical record: 2 cleared submissions from 2019 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Howmedica Osteonics Corp. (Aka Stryker Orthopaedics) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Howmedica Osteonics Corp. (Aka Stryker Orthopaedics)
2 devices