P040046S031

None

FDA Premarket Approval P040046 S031

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

DeviceP040046S031
Classification NameNone
Applicant
PMAP040046
SupplementS031

Supplemental Filings

Supplement NumberDateSupplement Type
P040046Original Filing
S032 2020-06-30 30-day Notice
S031
S030 2019-06-06 30-day Notice
S029 2018-07-02 30-day Notice
S028
S027 2017-12-18 135 Review Track For 30-day Notice
S026 2017-10-02 30-day Notice
S025 2017-07-20 30-day Notice
S024 2017-07-03 30-day Notice
S023 2017-06-07 30-day Notice
S022 2017-04-13 135 Review Track For 30-day Notice
S021 2017-03-01 Normal 180 Day Track
S020
S019 2016-11-23 Real-time Process
S018 2016-11-07 30-day Notice
S017 2016-09-07 Special (immediate Track)
S016 2016-05-24 Real-time Process
S015 2016-05-17 30-day Notice
S014 2015-12-30 Normal 180 Day Track No User Fee
S013 2014-12-30 Normal 180 Day Track
S012 2014-10-16 Normal 180 Day Track No User Fee
S011 2014-09-29 30-day Notice
S010
S009 2014-09-15 Normal 180 Day Track
S008 2014-08-11 Real-time Process
S007 2014-05-30 Normal 180 Day Track No User Fee
S006 2014-01-17 30-day Notice
S005 2014-01-02 Normal 180 Day Track No User Fee
S004 2013-06-12 30-day Notice
S003 2013-05-22 30-day Notice
S002 2013-05-20 30-day Notice
S001 2013-02-26 30-day Notice

NIH GUDID Devices

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