The following data is part of a premarket notification filed by Medtronic Vascular with the FDA for Dxterity, Dxterity Tra, Dxterity Angio-kit, Dxterity Ez-pak, Dxterity Tra Angio-kit, Dxterity Tra Ez-pak.
Device ID | K161287 |
510k Number | K161287 |
Device Name: | DxTerity, DxTerity TRA, DxTerity Angio-Kit, DxTerity EZ-Pak, DxTerity TRA Angio-Kit, DxTerity TRA EZ-Pak |
Classification | Catheter, Intravascular, Diagnostic |
Applicant | MEDTRONIC VASCULAR 37A CHERRY HILL DR Danvers, MA 01923 |
Contact | Nisarg Shah |
Correspondent | Nisarg Shah MEDTRONIC VASCULAR 37A CHERRY HILL DR Danvers, MA 01923 |
Product Code | DQO |
CFR Regulation Number | 870.1200 [🔎] |
Decision | Substantially Equivalent - Kit (SESK) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-05-09 |
Decision Date | 2016-08-19 |
Summary: | summary |