P990056S005

None

FDA Premarket Approval P990056 S005

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: P990056S005
• Classification Name: None
• PMA: P990056
• Supplement: S005

Supplemental Filings

Supplement Number	Date	Supplement Type
P990056		Original Filing
S038	2021-10-18	30-day Notice
S037	2019-11-14	Normal 180 Day Track
S036	2019-01-29	Real-time Process
S035	2018-10-26	Normal 180 Day Track No User Fee
S034	2018-10-01	30-day Notice
S033	2018-04-17	Real-time Process
S032	2018-04-03	30-day Notice
S031	2018-03-01	Real-time Process
S030
S029	2017-10-11	Real-time Process
S028	2017-07-31	Normal 180 Day Track
S027	2017-08-03	30-day Notice
S026	2017-05-24	30-day Notice
S025	2016-10-26	30-day Notice
S024	2016-09-07	Normal 180 Day Track No User Fee
S023	2016-02-18	30-day Notice
S022	2015-10-07	30-day Notice
S021	2014-04-04	Real-time Process
S020	2013-04-09	Real-time Process
S019	2012-11-30	30-day Notice
S018
S017	2012-02-29	30-day Notice
S016	2012-01-31	135 Review Track For 30-day Notice
S015	2011-11-22	30-day Notice
S014	2011-08-01	Normal 180 Day Track
S013	2011-05-03	Normal 180 Day Track No User Fee
S012	2011-04-25	30-day Notice
S011	2011-04-11	135 Review Track For 30-day Notice
S010	2009-10-07	135 Review Track For 30-day Notice
S009	2008-09-02	30-day Notice
S008	2008-03-28	Normal 180 Day Track
S007	2007-08-22	Normal 180 Day Track
S006	2006-12-28	30-day Notice
S005
S004	2006-10-05	Real-time Process
S003	2006-02-13	Normal 180 Day Track
S002	2006-01-23	Special (immediate Track)
S001	2001-10-09	Normal 180 Day Track

NIH GUDID Devices

Device ID	PMA	Supp
04015630921515	P990056	000
04015630920754	P990056	000
04015630920877	P990056	001
07613336154380	P990056	024
04015630921515	P990056	024
04015630920877	P990056	024
04015630939824	P990056	028
07613336165980	P990056	037
07613336165997	P990056	037
07613336166000	P990056	037
07613336167496	P990056	037
07613336217665	P990056	042