FLOSEAL MATRIX HEMOSTATIC AGENT FLOSEAL ENDOSCOPIC APPLICATOR

Agent, Absorbable Hemostatic, Collagen Based

FDA Premarket Approval P990009 S016

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

Approval for a modification to the endoscopic applicator and a modification of the "indication for use" for the endoscopic applicator. The device, as modified, will be marketed under the trade name floseal endoscopic applicator and is indicated for use in delivering floseal matrix hemostatic sealant to bleeding surgical sites through a 5 mm or larger trocar.

DeviceFLOSEAL MATRIX HEMOSTATIC AGENT FLOSEAL ENDOSCOPIC APPLICATOR
Classification NameAgent, Absorbable Hemostatic, Collagen Based
Generic NameAgent, Absorbable Hemostatic, Collagen Based
ApplicantBAXTER HEALTHCARE CORP.
Date Received2004-11-15
Decision Date2005-03-31
PMAP990009
SupplementS016
Product CodeLMF
Advisory CommitteeGeneral & Plastic Surgery
Supplement TypeReal-time Process
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product Yes
Applicant Address BAXTER HEALTHCARE CORP. 32650 N Wilson Rd round Lake, IL 60073

Supplemental Filings

Supplement NumberDateSupplement Type
P990009Original Filing
S071 2022-10-26 Special (immediate Track)
S070
S069 2022-04-22 30-day Notice
S068 2021-11-23 30-day Notice
S067
S066
S065 2020-11-27 30-day Notice
S064 2020-11-09 30-day Notice
S063 2020-08-19 30-day Notice
S062 2020-08-11 30-day Notice
S061
S060 2020-05-04 30-day Notice
S059 2019-12-10 30-day Notice
S058
S057 2019-07-01 30-day Notice
S056
S055
S054 2019-04-12 30-day Notice
S053 2019-01-22 Real-time Process
S052 2018-12-26 Real-time Process
S051 2018-12-04 Real-time Process
S050 2017-10-02 30-day Notice
S049 2017-08-14 Real-time Process
S048 2017-08-10 Real-time Process
S047
S046 2017-04-17 30-day Notice
S045 2016-12-05 Special (immediate Track)
S044 2016-11-02 Normal 180 Day Track
S043 2016-08-19 Special (immediate Track)
S042 2016-06-02 135 Review Track For 30-day Notice
S041 2015-06-15 30-day Notice
S040 2015-03-19 Normal 180 Day Track No User Fee
S039 2014-07-25 Normal 180 Day Track No User Fee
S038 2013-11-25 30-day Notice
S037 2013-06-06 Normal 180 Day Track
S036 2013-05-20 Special (immediate Track)
S035 2013-03-25 Normal 180 Day Track
S034 2012-03-06 Real-time Process
S033 2012-03-02 Real-time Process
S032 2011-04-06 30-day Notice
S031 2011-02-14 30-day Notice
S030 2010-07-21 30-day Notice
S029 2010-03-05 Special (immediate Track)
S028 2010-01-27 30-day Notice
S027 2009-10-15 Real-time Process
S026 2009-04-17 Real-time Process
S025 2009-02-26 Normal 180 Day Track
S024 2008-09-22 30-day Notice
S023 2008-09-12 30-day Notice
S022 2008-02-19 30-day Notice
S021 2007-11-19 30-day Notice
S020 2007-10-31 30-day Notice
S019 2007-02-20 Real-time Process
S018 2006-02-13 Normal 180 Day Track No User Fee
S017 2005-12-16 30-day Notice
S016 2004-11-15 Real-time Process
S015 2003-06-13 30-day Notice
S014 2003-04-29 Normal 180 Day Track No User Fee
S013 2002-11-18 Normal 180 Day Track
S012 2002-06-04 30-day Notice
S011 2001-09-25 Real-time Process
S010 2001-08-31 Normal 180 Day Track
S009 2001-06-26 Real-time Process
S008 2001-06-18 Normal 180 Day Track
S007 2001-03-05 Real-time Process
S006 2001-03-02 Real-time Process
S005 2001-02-01 Real-time Process
S004 2001-01-16 Real-time Process
S003 2000-12-22 Normal 180 Day Track
S002 2000-10-24 Normal 180 Day Track
S001 2000-10-04 Real-time Process

NIH GUDID Devices

Device IDPMASupp
50085412532863 P990009 044
50085412532733 P990009 044
50085412639609 P990009 051
50085412639593 P990009 051
50085412656309 P990009 053
50085412827952 P990009 067
50085412827891 P990009 070

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.