| |
| Trade Name | IMPELLA RP SYSTEM |
| Classification Name | right ventricular bypass (assist) device |
| Generic Name | right ventricular bypass (assist) device |
| Applicant |
| ABIOMED, INC. |
| 22 cherry hill dr. |
| danvers, MA 01923 |
|
| HDE Number | H140001 |
| Date Received | 09/10/2014 |
| Decision Date | 01/23/2015 |
| Product Code | |
| Docket Number | 15M-0267 |
| Notice Date | 02/09/2015 |
| Advisory Committee |
Cardiovascular |
| Clinical Trials |
NCT01777607
|
| Supplement Type | hde original |
| Expedited Review Granted? | No |
| Combination Product | No |
Approval Order Statement Approval for the impella rp system. This device is indicated for providing circulatory assistance for up to 14 days in pediatric or adult patients with a body surface area >=1. 5 m2 who develop acute right heart failure or decompensation following left ventricular assist device implantation, myocardial infarction, heart transplant, or open-heart surgery. |
| Approval Order | Approval Order |
| Summary | Summary of Safety And Probable Benefit |
| Labeling | Labeling Labeling Part 2 |
| Post-Approval Study | Show Report Schedule and Study Progress |
| Supplements: |
S001 S002 S003 S004 S005 S006 S007 S008 |