P120011S014

None

FDA Premarket Approval P120011 S014

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

DeviceP120011S014
Classification NameNone
Applicant
PMAP120011
SupplementS014

Supplemental Filings

Supplement NumberDateSupplement Type
P120011Original Filing
S024 2021-12-22 30-day Notice
S023
S022 2021-05-27 Normal 180 Day Track No User Fee
S021 2020-11-03 135 Review Track For 30-day Notice
S020 2020-07-02 30-day Notice
S019
S018 2020-03-17 30-day Notice
S017
S016 2019-06-21 30-day Notice
S015
S014
S013 2018-07-25 30-day Notice
S012 2018-06-11 Real-time Process
S011 2018-06-08 30-day Notice
S010 2017-10-23 Special (immediate Track)
S009 2017-10-05 Normal 180 Day Track No User Fee
S008 2016-10-04 30-day Notice
S007 2016-09-21 30-day Notice
S006 2016-07-28 Normal 180 Day Track No User Fee
S005 2016-04-15 30-day Notice
S004 2016-04-15 30-day Notice
S003 2016-03-28 135 Review Track For 30-day Notice
S002 2015-11-04 Normal 180 Day Track No User Fee
S001 2015-07-24 30-day Notice

NIH GUDID Devices

Device IDPMASupp
00850034511931 P120011 000
00850034511337 P120011 000
00850034511399 P120011 000
00850034511627 P120011 000
00850034511658 P120011 000
00850034511672 P120011 000
00850034511757 P120011 000
00850034511771 P120011 000
00850034511801 P120011 000
00850034511825 P120011 000
00850034511863 P120011 000
00850034511894 P120011 000
00850034511924 P120011 000
00850034511153 P120011 000

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