FDA 510(k) Applications Submitted by STRYKER TRAUMA GMBH
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K143063 |
10/24/2014 |
Stryker SonicPin System, Stryker SonicAnchor System |
STRYKER TRAUMA GMBH |
K170418 |
02/13/2017 |
Stryker SonicPin System |
Stryker Trauma Gmbh |
K180436 |
02/20/2018 |
T2 Alpha Tibia Nailing System, T2 Alpha Femur Antegrade GT/PF Nailing System, IMN Screws System, IMN Instruments System |
Stryker Trauma GmbH |
K191271 |
05/13/2019 |
T2 Alpha Femur Antegrade GT/PF Nailing System, T2 Alpha Tibia Nailing System, IMN Screws System, IMN Instruments System |
Stryker Trauma Gmbh |
K172774 |
09/14/2017 |
T2 Alpha Femur Antegrade GT/PF Nailing System, IMN Screws System, IMN Instruments System |
Stryker Trauma Gmbh |
K200869 |
04/01/2020 |
Gamma3 System |
Stryker Trauma GmbH |
K193308 |
11/29/2019 |
T2 Alpha Tibia Nailing System, IMN Screws System |
Stryker Trauma GmbH |
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