|
Device | PROTECTA DR/VR/XT DR/XT VR |
Generic Name | Implantable cardioverter defibrillator (non-CRT) |
Applicant | MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT 8200 CORAL SEA STREET N.E. MS MVS11 MOUNDS VIEW, MN 55112 |
PMA Number | P980016 |
Supplement Number | S289 |
Date Received | 04/04/2011 |
Decision Date | 05/05/2011 |
Product Code |
LWS |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement THE SUBJECT DEVICES ARE ABLE TO BE MANUFACTURED USING NEW PLATING LINES AT THE QUALIFIED SUPPLIER. |