| Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device. |
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| Trade Name | CADENCE FAMILY OF ICDS |
| Classification Name | pulse generator, permanent, implantable |
| Generic Name | transtelephonic follow-up/monitoring system |
| Applicant | ST. JUDE MEDICAL |
| PMA Number | P910023 |
| Supplement Number | S214 |
| Date Received | 06/23/2009 |
| Decision Date | 07/23/2009 |
| Product Code | |
| Advisory Committee |
Cardiovascular |
| Supplement Type | 30-day notice |
| Supplement Reason | process change: manufacturing |
| Expedited Review Granted? | No |
| Combination Product |
No
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Approval Order Statement Change in wafer test and hybrid test. |
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