Neuropro Spinaljaxx, Inc. is one of 18400 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuropro Spinaljaxx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Spinal Jaxx Interbody Fusion Device
1
Total
1
Cleared
0
Denied
Neuropro Spinaljaxx, Inc. has 1 FDA 510(k) cleared medical devices. Based in Modesto, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Neuropro Spinaljaxx, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Silver Pine Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Neuropro Spinaljaxx, Inc.
1 devices