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source DB |
source ID
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text
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size
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updated at |
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# proj.
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# Ann.
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updated_at |
| DevicePMAs@therightstef |
P980016_S668 |
Approval for an update to the indications for use to include pacing at the bundle of His. The device, as modified, will be marketed under the trade name SelectSecure MRI SureScan Lead Model 3830 and i |
459 Bytes |
2020-03-03 |
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10 |
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12 |
-
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| DevicePMAs@therightstef |
P980016_S062 |
Approval for the medtronic virtuoso dr/vr models d154a wg/d154vwc implantable cardioverter defibrillators and the concerto - virtuoso v 1.0 software application model sw002. The medtronic virtuoso dr |
1.81 KB |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P980023_S002 |
Approval for device hardware and software modifications. The device, as modified, will be marketed under the trade name mycroPhylax(Plus), Phylax XM, and TMS 1000(Plus) Tachyarrhythmia Monitoring Sys |
568 Bytes |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P920015_S017 |
Approval for the medtronic(r) sprint(tm) quattro(tm) model 6944 lead which is intended for single long-term use in the right ventricle. This lead has application for patients in which implantable car |
239 Bytes |
2020-03-03 |
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10 |
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4 |
-
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| DevicePMAs@therightstef |
P920015_S022 |
Approval for model 6726 df-1 y-adaptor/extender kit. The device is indicated to adapt two df-1 lead connectors to a single df-1 compatible connector port and/or will extend the length of a df-1 lead |
291 Bytes |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P910023_S066 |
Approval for the identity adx models xl dr 5386 and dr 5380 pulse generators and programmer software model 3307 v4.2a. These devices are indicated as follows: implantation of identity adx models5386 |
1.18 KB |
2020-03-03 |
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11 |
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0 |
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| DevicePMAs@therightstef |
P910073_S025 |
Approval for the Models 0144, 0145 and 0146 endocardial defibrillation leads. The device, as modified, will be marketed under the trade name ENDOTAK(R) ENDURANCE (Rx(TM)) Endocardial Defibrillation L |
389 Bytes |
2020-03-03 |
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11 |
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0 |
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| DevicePMAs@therightstef |
P980023_S023 |
Approval for a lead based on the kentrox sl and linox sd icd leads with 0.11 mm filaments in the lead tip conductor. The device, as modified, will be marketed under the trade name linox td implantabl |
476 Bytes |
2020-03-03 |
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11 |
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0 |
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| DevicePMAs@therightstef |
P980023_S019 |
Approval for modifications to the kentrox family of implantable cardioverter defibrillator (icd) leads. The devices, as modified, will be marketed under the trade names kentrox rv, kentrox rv steroid |
356 Bytes |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P950022_S041 |
Approval to modify the shock coil on the riata st optim and riata sts optim leads and to add two new passive lead models. The devices, as modified, will be marketed under the trade name riata st opti |
558 Bytes |
2020-03-03 |
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11 |
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0 |
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