K2 Medical GmbH & Co. KG is one of 490 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
K2 Medical GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs, K2 MEDICAL VASCULAR CLAMPS
2
Total
2
Cleared
0
Denied
K2 Medical GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Tuttlingen, DE.
Historical record: 2 cleared submissions from 2012 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by K2 Medical GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - K2 Medical GmbH & Co. KG
2 devices