P000021S007

None

FDA Premarket Approval P000021 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: P000021S007
• Classification Name: None
• PMA: P000021
• Supplement: S007

Supplemental Filings

Supplement Number	Date	Supplement Type
P000021		Original Filing
S044	2021-11-18	30-day Notice
S043	2020-09-14	30-day Notice
S042
S041	2019-06-19	30-day Notice
S040	2019-05-13	30-day Notice
S039	2018-09-28	Real-time Process
S038	2018-06-18	30-day Notice
S037	2018-04-17	30-day Notice
S036
S035	2017-11-20	30-day Notice
S034	2017-10-16	30-day Notice
S033	2017-09-25	Normal 180 Day Track No User Fee
S032	2017-06-20	30-day Notice
S031	2017-04-26	30-day Notice
S030	2017-02-17	30-day Notice
S029	2016-08-03	30-day Notice
S028	2015-12-07	Normal 180 Day Track
S027	2015-06-04	135 Review Track For 30-day Notice
S026	2014-08-27	30-day Notice
S025	2013-05-03	30-day Notice
S024	2012-10-31	30-day Notice
S023	2012-03-20	Real-time Process
S022	2012-03-08	30-day Notice
S021	2011-11-22	30-day Notice
S020	2011-06-30	Normal 180 Day Track
S019	2010-10-18	Real-time Process
S018	2010-08-19	Normal 180 Day Track
S017	2010-07-06	Real-time Process
S016	2010-03-25	30-day Notice
S015	2009-05-19	Normal 180 Day Track
S014	2009-04-06	Real-time Process
S013	2008-12-02	Normal 180 Day Track
S012	2008-03-03	Special (immediate Track)
S011	2008-02-26	30-day Notice
S010	2007-08-14	Real-time Process
S009	2006-12-06	30-day Notice
S008	2005-06-24	30-day Notice
S007
S006	2005-04-01	Special (immediate Track)
S005	2005-01-31	30-day Notice
S004	2004-11-15	Real-time Process
S003	2003-12-17	Real-time Process
S002	2002-03-26	Normal 180 Day Track
S001	2001-07-12	Real-time Process

NIH GUDID Devices

Device ID	PMA	Supp
00842768013874	P000021	001
00842768016660	P000021	013