P040003S020

None

FDA Premarket Approval P040003 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: P040003S020
• Classification Name: None
• PMA: P040003
• Supplement: S020

Supplemental Filings

Supplement Number	Date	Supplement Type
P040003		Original Filing
S021	2018-04-26	Real-time Process
S020
S019	2016-09-28	Special (immediate Track)
S018	2016-05-10	Real-time Process
S017	2016-04-04	Real-time Process
S016	2015-04-07	Normal 180 Day Track
S015	2015-03-04	Normal 180 Day Track
S014	2014-02-26	Normal 180 Day Track No User Fee
S013	2013-09-23	Real-time Process
S012	2012-08-13	30-day Notice
S011	2012-04-09	Special (immediate Track)
S010	2011-09-13	Normal 180 Day Track
S009	2010-07-26	Normal 180 Day Track No User Fee
S008	2010-07-01	Real-time Process
S007	2010-01-22	Normal 180 Day Track No User Fee
S006	2009-06-05	Normal 180 Day Track
S005	2008-09-19	Normal 180 Day Track
S004	2007-04-06	Normal 180 Day Track
S003
S002	2006-07-17	Normal 180 Day Track
S001	2005-08-25	Normal 180 Day Track No User Fee

NIH GUDID Devices

Device ID	PMA	Supp
07290015461047	P040003	017