| 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 | LIPOSORBER LA-15 System |
| Classification Name | apheresis for focal glomerulosclerosis in adult and pediatric patients |
| Generic Name | apheresis for focal glomerulosclerosis in adult and pediatric patients |
| Applicant |
| Kaneka Pharma America, LLC |
| 546 fifth ave., 21st floor |
| new york, NY 10036 |
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| HDE Number | H120005 |
| Supplement Number | S006 |
| Date Received | 04/13/2017 |
| Decision Date | 05/23/2017 |
| Product Code | |
| Advisory Committee |
Gastroenterology |
| Supplement Type | normal 75 day track |
| Supplement Reason | change design/components/specifications/material |
| Expedited Review Granted? | No |
| Combination Product | No |
Approval Order Statement Approval for changes to the housing of adsorption column la-15 and connector parts of tubing system nk-m3r(u), plus components of the liposorber® la-15 system. The device, as modified, will be marketed under the trade name liposorber® la-15 system and is indicated for use in the treatment of pediatric patients with nephrotic syndrome associated with primary focal segmental glomerulosclerosis when:1) standard treatment options, including corticosteroids and/or calcineurin inhibitortreatments, are unsuccessful or not well tolerated and the patient’s glomerular filtrationrate (gfr) >= 60 ml/min/1. 73 m2 or; 2) the patient is post renal transplantation. |
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