Pivotal Health Solutions is one of 16414 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pivotal Health Solutions - FDA 510(k) Cleared Devices
Recent clearances: ITRAC CERVICAL TRACTION SYSTEM, DECOMPRESSION OF CHOICE AND NEURO DECOMPRESSION DEVICE
2
Total
2
Cleared
0
Denied
Pivotal Health Solutions has 2 FDA 510(k) cleared medical devices. Based in Watertown, US.
Historical record: 2 cleared submissions from 2010 to 2014. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Pivotal Health Solutions 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 - Pivotal Health Solutions
2 devices