P030039S017

None

FDA Premarket Approval P030039 S017

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: P030039S017
• Classification Name: None
• PMA: P030039
• Supplement: S017

Supplemental Filings

Supplement Number	Date	Supplement Type
P030039		Original Filing
S027	2021-09-28	30-day Notice
S026	2021-04-21	Normal 180 Day Track
S025	2020-04-17	Real-time Process
S024
S023	2018-05-03	Real-time Process
S022	2018-02-20	30-day Notice
S021	2018-01-25	Special (immediate Track)
S020	2017-12-04	Normal 180 Day Track No User Fee
S019	2015-10-16	30-day Notice
S018
S017
S016	2010-06-01	Special (immediate Track)
S015	2010-03-02	Special (immediate Track)
S014	2009-09-04	Real-time Process
S013	2009-03-17	135 Review Track For 30-day Notice
S012	2008-11-07	30-day Notice
S011	2008-08-29	Special (immediate Track)
S010	2008-07-01	Real-time Process
S009	2008-03-24	30-day Notice
S008	2007-11-15	30-day Notice
S007	2007-10-31	30-day Notice
S006
S005	2007-06-25	30-day Notice
S004	2006-04-05	Normal 180 Day Track
S003	2006-02-02	Special (immediate Track)
S002	2006-01-17	Normal 180 Day Track No User Fee
S001	2003-12-18	Normal 180 Day Track No User Fee

NIH GUDID Devices

Device ID	PMA	Supp
35413765583415	P030039	024