Stryker Leibinger GmbH & Co KG - FDA 510(k) Cleared Devices
Recent clearances: MEDPOR Customized Implant Kit, Spine Guidance 5.4 Software, Spine Guidance 5.3 Software
22
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stryker Leibinger GmbH & Co KG Neurology ✕
2 devices