P040034S018

None

FDA Premarket Approval P040034 S018

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: P040034S018
• Classification Name: None
• PMA: P040034
• Supplement: S018

Supplemental Filings

Supplement Number	Date	Supplement Type
P040034		Original Filing
S035	2022-09-07	30-day Notice
S034	2021-10-18	30-day Notice
S033
S032	2020-08-17	30-day Notice
S031	2020-05-15	Real-time Process
S030	2019-12-30	Normal 180 Day Track No User Fee
S029	2019-06-11	30-day Notice
S028	2018-10-29	30-day Notice
S027	2017-11-30	Normal 180 Day Track No User Fee
S026	2017-07-21	30-day Notice
S025	2016-04-18	Real-time Process
S024	2014-07-08	Normal 180 Day Track
S023	2014-02-11	30-day Notice
S022
S021	2013-06-04	135 Review Track For 30-day Notice
S020	2011-08-25	135 Review Track For 30-day Notice
S019	2010-12-23	Special (immediate Track)
S018
S017	2010-08-20	30-day Notice
S016	2010-01-08	Normal 180 Day Track No User Fee
S015	2009-10-26	30-day Notice
S014	2009-10-13	Real-time Process
S013	2009-08-11	Real-time Process
S012	2009-07-29	30-day Notice
S011	2009-06-23	Normal 180 Day Track No User Fee
S010
S009	2007-05-15	Real-time Process
S008	2007-03-01	30-day Notice
S007	2006-08-24	Real-time Process
S006	2006-07-28	Normal 180 Day Track
S005	2006-06-13	Normal 180 Day Track No User Fee
S004	2006-06-08	Normal 180 Day Track
S003	2006-05-24	Normal 180 Day Track No User Fee
S002	2005-11-17	Real-time Process
S001	2005-09-01	Real-time Process

NIH GUDID Devices

Device ID	PMA	Supp
10381780000020	P040034	024
10381780000013	P040034	024