Surgical Innovations Group Plc is one of 491 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Surgical Innovations Group Plc - FDA 510(k) Cleared Devices
Recent clearances: FASTCLAMP ENDOSCOPIC CLAMPING SYSTEM, MODIFICATION TO: YELLOPORT PORT ACCESS SYSTEM
2
Total
2
Cleared
0
Denied
Surgical Innovations Group Plc has 2 FDA 510(k) cleared medical devices. Based in Leeds, GB.
Historical record: 2 cleared submissions from 2007 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgical Innovations Group Plc Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Surgical Innovations Group Plc
2 devices