Safeop Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Safeop Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: The EPAD 2 System
2
Total
2
Cleared
0
Denied
Safeop Surgical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Amherst, US.
Historical record: 2 cleared submissions from 2014 to 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Safeop Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Alphatec Spine, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Safeop Surgical, Inc.
2 devices