Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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Device | DUAL CHAMBER, IMPLANTABLE PULSE GENERATOR |
Generic Name | Implantable pulse generator, pacemaker (non-CRT) |
Applicant | MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT 8200 CORAL SEA STREET N.E. MOUNDS VIEW, MN 55112 |
PMA Number | P820003 |
Supplement Number | S089 |
Date Received | 02/06/2009 |
Decision Date | 03/06/2009 |
Product Code |
LWP |
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 TRANSFERRING THE FINAL IN-PROCESS INSPECTION AND FINAL PACKAGING PROCESS STEPS FOR THE MODEL 5409 POUCH-DISPOSABLE, 5PK TO THE CONTRACT MANUFACTURER¿S FACILITY IN MEDINA, MINNESOTA. |
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