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 |
|
|
