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Everflex Self-expanding Peripheral Stent System, E

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Everflex Self-expanding Peripheral Stent System, E manufactured by MEDTRONIC VASCULAR INC from https://fda.report/PMA/P110023S035

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Protg Gps Self Expanding Peripheral Stent System

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Protg Gps Self Expanding Peripheral Stent System manufactured by MEDTRONIC VASCULAR INC from https://fda.report/PMA/P060001S034

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Master Restore, Itrel, Synergy And Intellis Spinal

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Master Restore, Itrel, Synergy And Intellis Spinal manufactured by MEDTRONIC NEUROMODULATION from https://fda.report/PMA/P840001S521

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Zenith Dissection Endovascular System

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Zenith Dissection Endovascular System manufactured by WILLIAM COOK EUROPE APS from https://fda.report/PMA/P180001S005

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Activa Deep Brain Stimulation Therapy System, Perc

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Activa Deep Brain Stimulation Therapy System, Perc manufactured by MEDTRONIC Inc. from https://fda.report/PMA/P960009S432

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Capsurefix Mri Lead

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Capsurefix Mri Lead manufactured by Medtronic, Inc from https://fda.report/PMA/P090013S322

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Attain Ability Lead, Attain Performa Lead, Attain

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Attain Ability Lead, Attain Performa Lead, Attain manufactured by MEDTRONIC Inc. from https://fda.report/PMA/P080006S172

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Attain Bipolar Otw Lead,attain Otw Lv Lead, Consul

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Attain Bipolar Otw Lead,attain Otw Lv Lead, Consul manufactured by MEDTRONIC Inc. from https://fda.report/PMA/P010015S500

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Lifevest Wearable Defibrillator

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Lifevest Wearable Defibrillator manufactured by ZOLL MANUFACTURING CORPORATION from https://fda.report/PMA/P010030S159

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Adhesive, Capsure Sense Lead, Capsure Sp Lead, Cap

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Adhesive, Capsure Sense Lead, Capsure Sp Lead, Cap manufactured by MEDTRONIC CARDIAC RHYTHM DISEA from https://fda.report/PMA/P830061S207

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Percepta Bipolar Crt-p, Percepta Quadripolar Crt-p

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Percepta Bipolar Crt-p, Percepta Quadripolar Crt-p manufactured by MEDTRONIC Inc. from https://fda.report/PMA/P010015S501

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Bausch Lomb Ultra samfilcon A Visibility Tinte

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Bausch Lomb Ultra samfilcon A Visibility Tinte manufactured by Bausch and Lomb, Inc. from https://fda.report/PMA/P170035S017

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Cobalt Mri Icd, Cobalt Xt Mri Icd, Crome Mri Icd,

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Cobalt Mri Icd, Cobalt Xt Mri Icd, Crome Mri Icd, manufactured by MEDTRONIC CARDIAC RHYTHM DISEA from https://fda.report/PMA/P980016S823

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Capsurefix Lead, Capsurefix Novus Lead, Vitatron C

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Capsurefix Lead, Capsurefix Novus Lead, Vitatron C manufactured by Medtronic, Inc. from https://fda.report/PMA/P930039S243

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Transvene Cssvc Lead

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Transvene Cssvc Lead manufactured by MEDTRONIC Inc. from https://fda.report/PMA/P980050S138

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Adapta, Versa, Sensia Ipg, Advisa Dr Ipg, Advisa D

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Adapta, Versa, Sensia Ipg, Advisa Dr Ipg, Advisa D manufactured by MEDTRONIC Inc. from https://fda.report/PMA/P980035S718

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Capsure Sp Novus Lead, Capsure Sp Z Lead, Capsure

The Food and Drug Administration [FDA] has made public the pre-market approval [PMA] for Capsure Sp Novus Lead, Capsure Sp Z Lead, Capsure manufactured by MEDTRONIC CARDIAC RHYTHM DISEA from https://fda.report/PMA/P850089S162