|
Device | XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM, XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM |
Generic Name | Coronary drug-eluting stent |
Applicant | ABBOTT VASCULAR 3200 Lakeside Drive Santa Clara, CA 95054 |
PMA Number | P110019 |
Supplement Number | S078 |
Date Received | 09/24/2015 |
Decision Date | 10/22/2015 |
Product Code |
NIQ |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | Yes |
Approval Order Statement CHANGE TO THE ACCEPTANCE SAMPLING SYSTEM FOR DISLODGEMENT TESTING FOR THE XIENCE PRIME AND XIENCE PRIME II EVEROLIMUS ELUTING CORONARY STENT SYSTEM. |