P040013S007

None

FDA Premarket Approval P040013 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: P040013S007
• Classification Name: None
• PMA: P040013
• Supplement: S007

Supplemental Filings

Supplement Number	Date	Supplement Type
P040013		Original Filing
S025	2020-11-27	Real-time Process
S024	2020-04-17	Normal 180 Day Track No User Fee
S023	2020-03-24	Normal 180 Day Track No User Fee
S022	2019-03-21	Normal 180 Day Track No User Fee
S021	2015-06-22	Normal 180 Day Track No User Fee
S020	2015-01-21	Special (immediate Track)
S019	2014-05-05	135 Review Track For 30-day Notice
S018	2012-02-29	Special (immediate Track)
S017	2011-06-24	Normal 180 Day Track No User Fee
S016	2010-12-11	Normal 180 Day Track
S015	2009-08-14	Normal 180 Day Track No User Fee
S014	2009-07-06	Normal 180 Day Track No User Fee
S013	2008-03-26	Normal 180 Day Track
S012	2007-11-23	Normal 180 Day Track No User Fee
S011	2007-05-22	135 Review Track For 30-day Notice
S010
S009	2006-12-22	Special (immediate Track)
S008	2006-10-20	30-day Notice
S007
S006	2006-08-09	30-day Notice
S005	2006-07-31	Real-time Process
S004	2006-05-31	Normal 180 Day Track No User Fee
S003	2006-04-06	Normal 180 Day Track No User Fee
S002	2006-02-27	Real-time Process
S001

NIH GUDID Devices

Device ID	PMA	Supp
00850001118002	P040013	000