| |
| Trade Name | GATEWAY PTA BALLOON CATHETER |
| Classification Name | intracranial neurovascular stent |
| Generic Name | intracranial neurovascular stent |
| Applicant |
| Stryker Corp. |
| 47900 bayside pkwy. |
| fremont, CA 94538 |
|
| HDE Number | H050001 |
| Supplement Number | S050 |
| Date Received | 11/28/2012 |
| Decision Date | 04/11/2014 |
| Product Code | |
| Advisory Committee |
Neurology |
| Supplement Type | normal 75 day track |
| Supplement Reason | process change - manufacturer/sterilizer/packager/supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
Approval Order Statement Approval to eliminate certain testing requirements from the balloon component manufacturing process for the gateway pta balloon catheter. |