Spectranetics Corporation is one of 19218 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spectranetics Corporation - FDA 510(k) Cleared Devices
Recent clearances: TURBO-ELITE ATHERECTOMY CATHETERS, TURBO TANDEM SYSTEM, LEXIPLIANT DILATOR SHEATH SET
2
Total
2
Cleared
0
Denied
Spectranetics Corporation has 2 FDA 510(k) cleared medical devices. Based in Colorado Springs, US.
Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Spectranetics Corporation Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Spectranetics Corporation
2 devices