P880047S030

None

FDA Premarket Approval P880047 S030

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: P880047S030
• Classification Name: None
• PMA: P880047
• Supplement: S030

Supplemental Filings

Supplement Number	Date	Supplement Type
P880047		Original Filing
S052	2022-11-21	30-day Notice
S051
S050	2022-06-08	30-day Notice
S049	2021-12-20	30-day Notice
S048
S047
S046
S045	2021-09-29	30-day Notice
S044	2021-09-22	30-day Notice
S043
S042	2021-08-12	30-day Notice
S041	2021-08-02	30-day Notice
S040	2021-03-24	Special (immediate Track)
S039	2021-03-03	30-day Notice
S038	2020-10-06	30-day Notice
S037	2020-06-15	30-day Notice
S036	2020-04-22	30-day Notice
S035	2020-04-20	30-day Notice
S034	2020-01-03	30-day Notice
S033	2019-11-04	30-day Notice
S032	2019-06-24	30-day Notice
S031	2019-03-14	30-day Notice
S030
S029	2019-02-05	30-day Notice
S028	2018-12-07	Special (immediate Track)
S027	2017-06-12	30-day Notice
S026	2017-03-03	30-day Notice
S025	2016-09-26	Special (immediate Track)
S024	2016-08-29	30-day Notice
S023	2016-08-26	Special (immediate Track)
S022	2016-05-19	135 Review Track For 30-day Notice
S021	2015-06-19	30-day Notice
S020	2013-02-07	30-day Notice
S019	2012-03-14	30-day Notice
S018	2011-11-16	30-day Notice
S017	2011-07-20	30-day Notice
S016	2011-06-06	30-day Notice
S015	2011-04-18	Real-time Process
S014	2011-02-01	30-day Notice
S013	2009-05-06	30-day Notice
S012	2008-04-22	Normal 180 Day Track No User Fee
S011	2006-10-25	30-day Notice
S010	2006-02-28	Normal 180 Day Track
S009	2005-06-24	Normal 180 Day Track No User Fee
S008	2003-09-04	Normal 180 Day Track No User Fee
S007	1998-12-22	Normal 180 Day Track
S006	1998-08-28	Normal 180 Day Track
S005	1997-12-03	Normal 180 Day Track
S004	1995-09-05	Special (immediate Track)
S003	1993-11-03	Normal 180 Day Track
S002
S001	1990-03-09	Normal 180 Day Track

NIH GUDID Devices

Device ID	PMA	Supp
20705031147840	P880047	000
20705031005393	P880047	020