Medtronic Sofamor Danck USA, Inc. is one of 13048 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic Sofamor Danck USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: KYPHON (R) HV-R(R) Bone Cement, CD HORIZON Spinal System, ANATOMIC PEEK CERVICAL FUSION SYSTEM
4
Total
3
Cleared
0
Denied
Medtronic Sofamor Danck USA, Inc. has 3 FDA 510(k) cleared medical devices. Based in Memphis, US.
Historical record: 3 cleared submissions from 2011 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medtronic Sofamor Danck USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medtronic Sofamor Danek USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Medtronic Sofamor Danck USA, Inc.
4 devices