PMA_age_indications

Documents (2,236) JSON TSV

source DB	source ID	text	size	updated at	# proj.	updated_at
DevicePMAs@therightstef	P960040_S026	Approval for the ventak prizm 2 vr/dr models 1860/1861, ventak prizm vr/dr models 1850/1851/1855/1856, ventak prizm vr/dr he models 1852/1853, ventak mini iv models 1790/1793/1796 and ventak mini iii	598 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P960040_S031	Approval for the vitality ds vr model t135, vitality ds model t125, and vitality el model t127 implantable cardioverter defibrillator systems and the programmer software application model 2844 version	1000 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P960040_S022	Approval for model 2725 ventak(r) prizm(tm) diagnostic/restoration tool version 1.5. The device is indicated to diagnose and restore to factory normal settings ventak prizm/prizm he devices that have	275 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P980035_S384	Approval for the mycarelink smart monitor used with the device. The device, as modified, will be marketed under the trade name mycarelink smart monitor andthe mycarelink heart application and is indi	639 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P090013_S000	Approval for the revo mrisurescan pacing system, which consists of the medtronic revo mri surescan model rvdr01 ipg, the medtronic capsurefix mri surescan 5086mri lead, and the revo mri software appli	1.14 KB	2020-03-03	11	-
DevicePMAs@therightstef	P090013_S149	Approval for the mycarelink smart monitor used with the device. The device, as modified, will be marketed under the trade name mycarelink smart monitor and the mycarelink heart application and is ind	641 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P960040_S028	Approval for the vantak prizm avt aicd system. The device is indicated for use in the following: patients who are icd indicated and who have atrial tachyarrhythmias, or who are at risk of developing	629 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P960040_S051	Approval for the vitality he model t182 implantable cardioverter defibrillator (icd) system and the consult programmer software application model 2896 version 1.0. The device is indicated for use as	309 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P010015_S016	Approval for modifications to the device labeling to describe the care-hf clinical study. medtronic also requests a reformatting of the indications statement and the addition of a clinical outcomes se	904 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P960040_S053	Approval for the vitality he model t180 implantable cardioverter defibrillator (icd) system and the consult programmer software application model 2896 version 1.0. The device is indicated as follows:	373 Bytes	2020-03-03	11	-