P980041S020

None

FDA Premarket Approval P980041 S020

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: P980041S020
• Classification Name: None
• PMA: P980041
• Supplement: S020

Supplemental Filings

Supplement Number	Date	Supplement Type
P980041		Original Filing
S049	2020-09-30	Real-time Process
S048	2020-07-22	Real-time Process
S047	2020-06-23	Real-time Process
S046	2019-12-18	Real-time Process
S045	2019-05-13	Real-time Process
S044	2019-05-02	Real-time Process
S043
S042
S041	2018-09-25	Real-time Process
S040	2018-08-13	30-day Notice
S039	2017-09-28	30-day Notice
S038
S037	2017-06-09	30-day Notice
S036	2017-03-22	Real-time Process
S035	2017-01-17	30-day Notice
S034	2016-06-10	135 Review Track For 30-day Notice
S033	2015-06-05	30-day Notice
S032	2015-05-07	Real-time Process
S031	2014-11-10	30-day Notice
S030	2014-11-04	135 Review Track For 30-day Notice
S029	2014-08-25	Real-time Process
S028	2014-08-25	135 Review Track For 30-day Notice
S027	2013-12-17	Real-time Process
S026	2013-09-26	Special (immediate Track)
S025	2013-06-13	Special (immediate Track)
S024	2013-04-12	Special (immediate Track)
S023	2013-03-29	Real-time Process
S022	2013-01-23	Real-time Process
S021	2013-01-03	30-day Notice
S020
S019
S018	2012-10-25	Special (immediate Track)
S017	2012-03-15	Special (immediate Track)
S016	2011-12-23	Real-time Process
S015	2011-01-12	Special (immediate Track)
S014	2011-01-10	Special (immediate Track)
S013	2010-09-27	Normal 180 Day Track
S012	2008-05-27	Real-time Process
S011	2008-02-26	Special (immediate Track)
S010	2007-09-07	Real-time Process
S009	2007-05-30	Normal 180 Day Track
S008	2006-04-10	Real-time Process
S007	2006-01-18	30-day Notice
S006	2004-07-29	Real-time Process
S005	2004-07-01	30-day Notice
S004	2003-12-02	Normal 180 Day Track No User Fee
S003	2002-12-04	Real-time Process
S002	2002-07-22	Normal 180 Day Track
S001	2002-06-18	Normal 180 Day Track