|
Device | CAPSUREFIX & CRYSTALLINE ACT FIX |
Generic Name | Permanent defibrillator electrodes |
Applicant | Medtronic, Inc. 8200 CORAL SEA STREET N.E. MOUNDS VIEW, MN 55112 |
PMA Number | P930039 |
Supplement Number | S055 |
Date Received | 06/01/2011 |
Decision Date | 06/29/2011 |
Product Code |
NVY |
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 A LEAD ASSEMBLY CRIMPING PROCESS IMPROVEMENT. |