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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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1 to 10 of 500 Results *
Applicant: MEDTRONIC INC Product Code: LWS Decision Date to 04/18/2015
 
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Device Name
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Applicant
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PMA
Number
Sort by PMA Number [0-9]
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Decision
Date
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SPRINT QUATTRO LEAD medtronic inc. P920015 S150 04/02/2015
MAXIMO II, PROTECTA, PROTECTA XT, SECURA medtronic inc. P980016 S521 03/30/2015
EVERA S DR ICD, EVERA S VR ICD, EVERA XT medtronic inc. P980016 S534 03/19/2015
EVERA S DR ICD, EVERA S VR ICD, EVERA XT medtronic inc. P980016 S531 03/17/2015
EVERA S DR,EVERA S VR,EVERA XT DR,EVERA medtronic inc. P980016 S533 03/17/2015
EVERA S(DR/VR) ICD, EVERA XT (DR/VR) ICD medtronic inc. P980016 S526 03/04/2015
SPRINT QUATTRO LEAD medtronic inc. P920015 S148 03/03/2015
EVERA S DR, EVERA S VR, EVERA XT DR,EVER medtronic inc. P980016 S528 03/03/2015
SPRINT QUATRO LEAD,SUBCUTANEOUS LEAD medtronic inc. P920015 S149 03/02/2015
TRANSVENE CS/SVC LEAD medtronic inc. P980050 S098 03/02/2015

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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