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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 |