|
Device | EDWARDS SAPIEN TRANSCATHETER HEART VALVE AND ACCESSORIES |
Generic Name | Aortic valve, prosthesis, percutaneously delivered |
Applicant | EDWARDS LIFESCIENCES, LLC. One Edwards Way Irvine, CA 92614 |
PMA Number | P100041 |
Date Received | 11/01/2010 |
Decision Date | 11/02/2011 |
Withdrawal Date
|
03/18/2019 |
Product Code |
NPT |
Docket Number | 11M-0837 |
Notice Date | 11/22/2011 |
Advisory Committee |
Cardiovascular |
Clinical Trials | NCT00530894
|
Expedited Review Granted? | Yes |
Combination Product | No |
Recalls | CDRH Recalls |
Approval Order Statement APPROVAL FOR THE SAPIEN TRANSCATHETER HEART VALVE, MODEL 9000TFX, SIZES 23MM AND 26MM AND ACCESSORIES. THIS DEVICE IS INDICATED FOR TRANSFEMORAL DELIVERY IN PATIENTS WITH SEVERE SYMPTOMATIC NATIVE AORTIC VALVE STENOSIS WHO HAVE BEEN DETERMINED BY A CARDIAC SURGEON TO BE INOPERABLE FOR OPEN AORTIC VALVE REPLACEMENT AND IN WHOM EXISTING COMORBIDITIES WOULD NOT PRECLUDE THE EXPECTED BENEFIT FROM CORRECTION OF THE AORTIC STENOSIS. |
Approval Order | Approval Order |
Summary | Summary of Safety and Effectiveness |
Labeling | Labeling
|
Post-Approval Study | Show Report Schedule and Study Progress |
Supplements: |
S001 S002 S003 S004 S005 S006 S007 S008 S009 S010 S011 S012 S013 S014 S015 S016 S017 S018 S019 S020 S021 S022 S023 S024 S027 S028 S029 S030 S031 S032 S033 S034 S035 S036 S037 S038 S039 S040 S041 S042 S043 S044 S046 S047 S048 S049 S050 S051 S052 S053 S054 S055 S056 S058 S059 S060 S061 S062 S063 S064 S065 S066 S068 S069 |