Spectranetrics is one of 19553 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spectranetrics - FDA 510(k) Cleared Devices
Recent clearances: AngioSculpt PTA Scoring Baloon Catheters
1
Total
1
Cleared
0
Denied
Spectranetrics has 1 FDA 510(k) cleared medical devices. Based in Colorado Springs, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Spectranetrics Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Spectranetics as regulatory consultant.
FDA 510(k) Regulatory Record - Spectranetrics
1 devices