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 |