| 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 | PHILOS DR ACC PACING SYSTEM AND PROGRAMMER SOFTWARE VERSION B-KAC.V.U/1 |
| Classification Name | implantable pacemaker pulse-generator |
| Generic Name | external dual-chamber pacemaker |
| Regulation Number | 870.3610 |
| Applicant | BIOTRONIK, INC. |
| PMA Number | P950037 |
| Supplement Number | S030 |
| Date Received | 01/09/2003 |
| Decision Date | 08/04/2003 |
| Product Code | |
| Advisory Committee |
Cardiovascular |
| Supplement Type | normal 180 day track |
| Supplement Reason | labeling change - performance characteristics |
| Expedited Review Granted? | No |
| Combination Product |
No
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Approval Order Statement Approval for a modified philos dr pacing system. The device, as modified, will be marketed under the trade name philos dr acc pacing system and programmer software version b-kac. V. U/1 and is indicated for use in patients with standard bradycardia pacing indications. Rate-adaptive pacing with the philos dr acc pulse generator is indicated for patients exhibiting chronotropic incompetence and who would benefit from increased pacing rates concurrent with physical activity. Generally accepted indications for long-term cardiac pacing include, but are not limited to: sick sinus syndrome (i. E. Bradycardia-tachycardia syndrome, sinus arrest, sinus bradycardia), sino-atrial (sa) block, second- and third- degree av block, and carotid sinus syndrome. Patients who demonstrate hemodynamic benefit through maintenance of av synchrony should be considered for one of the dual chamber or atrial pacing modes. Dual chamber modes are specifically indicated for treatment of conduction disorders that require both restoration of rate and av synchrony such as av nodal disease, diminished cardiac output or congestive heart failure associated with conduction disturbances, and tachyarrhythmias that are suppressed by chronic pacing. |
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