|
Device | LUTONIX DRUG COATED BALLOON PTA CATETER |
Generic Name | Drug-Eluting Peripheral Transluminal Angioplasty Catheter |
Applicant | LUTONIX 9409 SCIENCE CENTER DR NEW HOPE, MN 55428 |
PMA Number | P130024 |
Date Received | 11/25/2013 |
Decision Date | 10/09/2014 |
Product Code |
ONU |
Docket Number | 14M-1597 |
Notice Date | 10/14/2014 |
Advisory Committee |
Cardiovascular |
Clinical Trials | NCT00930813
|
Expedited Review Granted? | Yes |
Combination Product | Yes |
Approval Order Statement APPROVAL FOR THE LUTONIX 035 DRUG COATED BALLOON PTA CATHETER (LUTONIX DCB). THIS DEVICE IS INDICATED FOR PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY, AFTER PRE-DILATATION, OF DE NOVO OR RESTENOTIC LESIONS UP TO 150MM IN LENGTH IN NATIVE SUPERFICIAL FEMORAL OR POPLITEAL ARTERIES WITH REFERENCE VESSELDIAMETERS OF 4-6MM. |
Approval Order | Approval Order |
Summary | Summary of Safety and Effectiveness |
Labeling | Labeling Labeling Part 2 |
Post-Approval Study | Show Report Schedule and Study Progress |
Supplements: |
S014 S005 S008 S002 S009 S010 S012 S017 S006 S003 S004 S001 S007 S011 S013 S018 S015 S029 S035 S036 S040 S038 S022 S021 S020 S023 S024 S026 S027 S030 S031 S032 S033 S037 S034 S025 S042 S041 S043 |