Stryker Corporate - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Stryker Corporate has 6 FDA 510(k) cleared medical devices. Based in Freiburg, Baden-Wuerttemberg, DE.
Historical record: 6 cleared submissions from 2013 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Stryker Corporate Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Stryker Corporate
6 devices
Cleared
Jul 07, 2016
Styrker OrthoMap Express Knee System
Orthopedic
241d
Cleared
Sep 04, 2015
Navigated XIA 4.5 Polyaxial Screwdriver
Orthopedic
260d
Cleared
Oct 31, 2014
SPINEMASK TRACKER, SPINEMAP 3D 3.0-SOFTWARE,SPINEMAP 3D 3.0-UPGREADE,...
Orthopedic
106d
Cleared
Sep 08, 2014
PROFESS SOFTWARE, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 70...
Ear, Nose, Throat
89d
Cleared
Oct 18, 2013
CRANIAL MAP NEURO
Neurology
172d
Cleared
Sep 27, 2013
STRYKER NAV3I PLATFORM
Neurology
182d