| Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the Original HDE to get an up-to-date view of this device. |
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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 |
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| HDE Number | H140001 |
| Supplement Number | S001 |
| Date Received | 02/09/2015 |
| Decision Date | 03/03/2015 |
| Product Code | |
| Advisory Committee |
Cardiovascular |
| Supplement Type | normal 75 day track |
| Supplement Reason | request for adn |
| Expedited Review Granted? | No |
| Combination Product | No |
Approval Order Statement Approval in accordance with 613(b) of the food and drug administrationsafety and innovation act (fdasia), a determination that your humanitarian use device (hud) meets the conditions of either subclause (i) or (ii) under section 520(m)(6)(a)(i) of the federal food, drug, and cosmetic act (fd&c act), as amended by the fdasia, so that your devicemay be sold for an amount that exceeds the costs of research and development, fabrication, and distribution of the device (i. E. , for profit). The adn for this device has been determined to be 4,000. |
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