MODEL 6577 STERILIZABLE TELEMETRY WAND

Implantable Cardioverter Defibrillator (non-crt)

FDA Premarket Approval P830060 S026

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Premarket approval (pma) // quick links: skip to main page content skip to search skip to topics menu skip to common links u. S. Food & drug administration follow fda en español search fda home food drugs medical devices radiation-emitting products vaccines, blood & biologics animal & veterinary cosmetics tobacco products premarket approval (pma) var mp = { version: '1. 0. 22', domains: {'es':'esp. Fda. Gov'}, srclang: 'en', urllang: 'mp_js_current_lang', srcurl: unescape('mp_js_orgin_url'), init: function(){ if (mp. Urllang. Indexof('p_js_')==1) { mp. Srcurl=window. Top. Document. Location. Href; mp. Urllang=mp. Srclang; } }, getcookie: function(name){ var start=document. Cookie. Indexof(name+'='); if(start < 0) return null; start=start+name. Length+1; var end=document. Cookie. Indexof(';', start); if(end < 0) end=document. Cookie. Length; while (document. Cookie. Charat(start)==' '){ start++; } return unescape(document. Cookie. Substring(start,end)); }, setcookie: function(name,value,path,domain){ var cookie=name+'='+escape(value); if(path)cookie+='; path='+path; if(domain)cookie+='; domain='+domain; var now=new date(); now. Settime(now. Gettime()+1000*60*60*24*365); cookie+='; expires='+now. Toutcstring(); document. Cookie=cookie; }, switchlanguage: function(lang){ if(lang! =mp. Srclang){ var script=document. Createelement('script'); script. Src=location. Protocol+'//'+mp. Domains[lang]+'/'+mp. Srclang+lang+'/? 1023749632;'+encodeuricomponent(mp. Srcurl); document. Body. Appendchild(script); } else if(lang==mp. Srclang && mp. Urllang! =mp. Srclang){ var script=document. Createelement('script'); script. Src=location. Protocol+'//'+mp. Domains[mp. Urllang]+'/'+mp. Srclang+mp. Urllang+'/? 1023749634;'+encodeuricomponent(location. Href); document. Body. Appendchild(script); } return false; }, switchtolang: function(url) { window. Top. Location. Href=url; } }; var addthis_config = {data_track_clickback: true, ui_508_compliant: true, services_compact: 'facebook, twitter, linkedin, pinterest_share, email', services_exclude: 'print', image_container: "#user_provided" } ; fda home medical devices databases -. Pma { color: #000000; width: 900px; float: right; margin: 0px 25px 0px 0px; }. Pma-left { color: #000000; float: left; width: 610px; margin: 9px 30px 0px 0; }. Pma-right { color: #000000; float: right; width: 190px; margin: 9px 18px 0 0; padding: 8px 12px 10px 12px; background-color: #f3f3f3; border: 1px solid #b0b0b0; border-radius: 6px; }. Pma-intro { margin: 0 0 18px 0; padding: 5px 12px 12px 12px; background-color: #e8eff5; border: 1px solid #b0b0b0; border-radius: 6px; } #pma-form { table-layout:fixed; width: 610px; font-size: 11px; border: 1px solid #b0b0b0; } #pma-form-title{ padding: 6px 6px 6px 6px; width: 100%; background-color: #e8eff5; border-bottom: 1px solid #b0b0b0; margin-top: 0px; } #pma-form-title-left { font-size: 13px; font-weight: bold; } #pma-form-title-right { font-size: 11px; padding: 0px 0px 0px 300px; } #pma-results-table { table-layout:fixed; width: 610px; border-color: #b0b0b0; border-width: 0 0 1px 1px; border-style: solid; } #pma-results-table th { padding: 6px 12px; background-color: #e8eff5; border-color: #b0b0b0; border-width: 1px 1px 0 0; border-style: solid; font-size: 12px; } #pma-results-table td { padding: 6px 12px; border-color: #b0b0b0; border-width: 1px 1px 0 0; border-style: solid; text-transform: capitalize; } #pma-results-table tr:nth-child(odd) { background-color: #f3f3f3; }. Sort { float: right; margin-top: 5px;}. Sort a { color: #484138; }. Sort a:hover { color: #0f2a8c; }

DeviceMODEL 6577 STERILIZABLE TELEMETRY WAND
Classification NameImplantable Cardioverter Defibrillator (non-crt)
Generic NameImplantable Cardioverter Defibrillator (non-crt)
ApplicantBOSTON SCIENTIFIC
Date Received1991-07-05
Decision Date1991-11-20
PMAP830060
SupplementS026
Product CodeLWS
Docket NumberPremarket Approval (PMA) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices Radia
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address BOSTON SCIENTIFIC 4100 Hamline Avenue North st. Paul, MN 55112

Supplemental Filings

Supplement NumberDateSupplement Type
P830060Original Filing
S088 2022-11-01 30-day Notice
S087 2021-09-30 30-day Notice
S086 2021-04-30 30-day Notice
S085 2021-03-08 30-day Notice
S084 2021-02-24 Normal 180 Day Track No User Fee
S083 2019-03-13 30-day Notice
S082 2018-03-26 30-day Notice
S081 2016-05-27 30-day Notice
S080 2014-06-30 30-day Notice
S079 2014-04-22 30-day Notice
S078 2014-03-04 Real-time Process
S077 2014-02-21 Real-time Process
S076 2013-08-29 30-day Notice
S075 2013-05-16 Real-time Process
S074 2012-11-08 30-day Notice
S073 2012-10-10 30-day Notice
S072 2012-07-26 Real-time Process
S071
S070 2012-03-26 30-day Notice
S069 2011-05-25 30-day Notice
S068 2011-04-01 30-day Notice
S067 2011-03-28 Real-time Process
S066
S065 2009-12-18 30-day Notice
S064 2009-12-16 30-day Notice
S063
S062 2009-02-24 Normal 180 Day Track
S061
S060 2006-04-13 30-day Notice
S059 2006-04-13 30-day Notice
S058 2005-05-27 Special (immediate Track)
S057 2004-12-03 30-day Notice
S056 2004-10-21 30-day Notice
S055 2004-06-14 30-day Notice
S054 2004-04-14 30-day Notice
S053 2004-01-13 30-day Notice
S052 2003-10-30 Special (immediate Track)
S051 2002-11-13 30-day Notice
S050
S049 2000-08-21 Normal 180 Day Track
S048 2000-04-27 Real-time Process
S047 2000-01-11 Real-time Process
S046 1999-12-16 Normal 180 Day Track
S045 1999-08-25 Normal 180 Day Track
S044 1998-11-20 Real-time Process
S043 1998-10-13 Real-time Process
S042 1996-10-16 Normal 180 Day Track
S041 1995-12-21 Normal 180 Day Track
S040 1995-02-10 Normal 180 Day Track
S039 1995-05-01 Normal 180 Day Track
S038 1995-04-06 Normal 180 Day Track
S037 1994-12-23 Normal 180 Day Track
S036 1994-12-14 Normal 180 Day Track
S035 1994-04-20 Normal 180 Day Track
S034 1993-10-19 Normal 180 Day Track
S033 1993-04-15 Normal 180 Day Track
S032 1992-08-26 Normal 180 Day Track
S031
S030 1992-04-29 Normal 180 Day Track
S029 1991-11-22 Normal 180 Day Track
S028 1991-11-07 Normal 180 Day Track
S027 1991-09-23 Normal 180 Day Track
S026 1991-07-05 Normal 180 Day Track
S025 1991-05-15 Normal 180 Day Track
S024 1990-11-13 Normal 180 Day Track
S023 1990-09-27 Normal 180 Day Track
S022 1990-09-26 Normal 180 Day Track
S021 1990-08-15 Normal 180 Day Track
S020 1990-07-23 Normal 180 Day Track
S019 1990-05-04 Normal 180 Day Track
S018 1990-03-07 Normal 180 Day Track
S017
S016 1990-03-01 Normal 180 Day Track
S015 1990-02-15 Normal 180 Day Track
S014 1990-02-15 Normal 180 Day Track
S013 1989-11-20 Normal 180 Day Track
S012 1989-10-31 Normal 180 Day Track
S011 1989-10-17 Normal 180 Day Track
S010 1989-10-12 Normal 180 Day Track
S009
S008 1989-06-13 Normal 180 Day Track
S007 1988-08-15 Normal 180 Day Track
S006 1988-03-08 Normal 180 Day Track
S005 1987-09-22 Normal 180 Day Track
S004 1986-09-16 Normal 180 Day Track
S003 1986-08-06 Special (immediate Track)
S002 1986-02-03
S001 1985-12-03

NIH GUDID Devices

Device IDPMASupp
00802526489303 P830060 000
00802526067310 P830060 000
00802526489600 P830060 000
00802526489563 P830060 000
00802526489280 P830060 000
00802526489594 P830060 023
00802526489587 P830060 023
00802526489730 P830060 045
00802526489723 P830060 045
00802526067518 P830060 067
00802526064395 P830060 077
00802526617300 P830060 084
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