Stryker Trauma AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stryker Trauma AG - FDA 510(k) Cleared Devices
25
Total
25
Cleared
0
Denied
Stryker Trauma AG has 25 FDA 510(k) cleared orthopedic devices. Based in Malwah, US.
Historical record: 25 cleared submissions from 2013 to 2017.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stryker Trauma AG
25 devices
Cleared
Oct 02, 2017
ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder...
Orthopedic
70d
Cleared
Dec 28, 2015
Asnis JFX System
Orthopedic
56d
Cleared
Jun 24, 2015
VariAx 2 Wrist Fusion System
Orthopedic
51d
Cleared
Dec 22, 2014
AxSOS 3 Ti Locking Plate System
Orthopedic
49d
Cleared
Nov 10, 2014
HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM
Orthopedic
209d
Cleared
Aug 07, 2014
VARIAX 2 SYSTEM
Orthopedic
16d
Cleared
Jul 22, 2014
VARIAX ELBOW PLATING SYSTEM
Orthopedic
29d
Cleared
Jun 20, 2014
AXSOS 3 TI LOCKING PLATE SYSTEM
Orthopedic
51d
Cleared
Jun 20, 2014
VARIAX 2 ONE THIRD TUBULAR PLATING SYSTEM
Orthopedic
42d
Cleared
May 29, 2014
VARIAX 2 COMPRESSION PLATING SYSTEM
Orthopedic
85d
Cleared
Apr 17, 2014
VARIAX 2 SYSTEM
Orthopedic
21d
Cleared
Apr 03, 2014
VARIAX 2 SYSTEM
Orthopedic
48d