P950009S007

None

FDA Premarket Approval P950009 S007

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

• Device: P950009S007
• Classification Name: None
• PMA: P950009
• Supplement: S007

Supplemental Filings

Supplement Number	Date	Supplement Type
P950009		Original Filing
S026	2022-06-15	30-day Notice
S025	2021-09-02	Real-time Process
S024	2021-03-04	30-day Notice
S023	2019-11-19	30-day Notice
S022	2019-06-05	Normal 180 Day Track
S021	2016-05-19	30-day Notice
S020	2016-03-07	Normal 180 Day Track No User Fee
S019	2015-04-24	Real-time Process
S018	2014-11-12	Normal 180 Day Track
S017	2013-12-02	Real-time Process
S016	2012-07-05	Real-time Process
S015	2012-03-28	Normal 180 Day Track
S014	2012-01-17	Real-time Process
S013	2011-09-15	Real-time Process
S012	2010-08-17	Special (immediate Track)
S011	2009-12-10	30-day Notice
S010	2009-06-25	Normal 180 Day Track No User Fee
S009	2009-03-26	Real-time Process
S008	2007-10-02	Panel Track
S007
S006
S005	2001-10-26	Real-time Process
S004	1999-10-01	Normal 180 Day Track
S003	1998-10-13	Normal 180 Day Track
S002	1996-06-06	Panel Track
S001	1995-11-06	Special (immediate Track)

NIH GUDID Devices

Device ID	PMA	Supp
00382904901899	P950009	008
00382904910877	P950009	015
00382904910860	P950009	015
00382904910853	P950009	015
00382904910907	P950009	015
00382904914646	P950009	022