Incite Innovation is one of 18461 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Incite Innovation - FDA 510(k) Cleared Devices
Recent clearances: INCITE ANCHORED CERVICAL INTERBODY DEVICE
1
Total
1
Cleared
0
Denied
Incite Innovation has 1 FDA 510(k) cleared medical devices. Based in Springfield, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Incite Innovation 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 - Incite Innovation
1 devices