Ackermann Instrumente GmbH is one of 18502 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ackermann Instrumente GmbH - FDA 510(k) Cleared Devices
Recent clearances: Ackermann Intervertebral Body Fusion Device, ACKERMANN EUROPCLIP, ACKERMANN SURGICAL INSTRUMENTS
3
Total
3
Cleared
0
Denied
Ackermann Instrumente GmbH has 3 FDA 510(k) cleared medical devices. Based in Chesterland, US.
Historical record: 3 cleared submissions from 1998 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ackermann Instrumente GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ferguson Medical International Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ackermann Instrumente GmbH
3 devices