P060035S028

None

FDA Premarket Approval P060035 S028

This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.

Pre-market Approval Supplement Details

DeviceP060035S028
Classification NameNone
Applicant
PMAP060035
SupplementS028

Supplemental Filings

Supplement NumberDateSupplement Type
P060035Original Filing
S030 2020-03-16 Normal 180 Day Track No User Fee
S029 2020-03-16 Normal 180 Day Track No User Fee
S028
S027 2018-10-22 30-day Notice
S026 2018-06-01 Normal 180 Day Track
S025 2015-07-16 30-day Notice
S024 2014-11-13 30-day Notice
S023 2014-09-19 30-day Notice
S022 2013-10-30 30-day Notice
S021 2013-10-28 30-day Notice
S020 2013-02-15 30-day Notice
S019 2013-02-11 30-day Notice
S018 2012-11-19 30-day Notice
S017 2012-11-15 30-day Notice
S016 2012-11-13 30-day Notice
S015 2012-11-01 30-day Notice
S014 2012-08-03 30-day Notice
S013 2011-11-23 Special (immediate Track)
S012 2011-10-28 30-day Notice
S011 2011-10-28 135 Review Track For 30-day Notice
S010 2011-09-07 Special (immediate Track)
S009 2011-05-25 30-day Notice
S008 2011-05-04 Normal 180 Day Track No User Fee
S007 2011-04-18 30-day Notice
S006 2011-02-17 Normal 180 Day Track No User Fee
S005 2011-01-10 135 Review Track For 30-day Notice
S004 2010-12-22 Special (immediate Track)
S003 2010-11-01 Normal 180 Day Track No User Fee
S002 2010-08-02 Normal 180 Day Track No User Fee
S001 2009-01-08 Normal 180 Day Track

NIH GUDID Devices

Device IDPMASupp
00380740011154 P060035 001
00380740011147 P060035 001
00380740011130 P060035 001
00380740146177 P060035 026
00380740145187 P060035 026
00380740130282 P060035 026

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