P110022S007

None

FDA Premarket Approval P110022 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: P110022S007
• Classification Name: None
• PMA: P110022
• Supplement: S007

Supplemental Filings

Supplement Number	Date	Supplement Type
P110022		Original Filing
S028	2021-12-02	30-day Notice
S027	2018-10-26	Normal 180 Day Track No User Fee
S026	2018-10-09	30-day Notice
S025	2018-04-17	Real-time Process
S024	2017-10-11	Real-time Process
S023	2017-08-03	30-day Notice
S022	2017-07-06	Normal 180 Day Track
S021	2017-05-24	30-day Notice
S020	2016-12-07	Real-time Process
S019	2016-09-07	Normal 180 Day Track No User Fee
S018	2016-07-11	135 Review Track For 30-day Notice
S017	2016-02-16	30-day Notice
S016	2016-01-27	30-day Notice
S015	2016-01-27	135 Review Track For 30-day Notice
S014	2015-10-07	30-day Notice
S013	2014-10-16	Real-time Process
S012	2014-04-04	Real-time Process
S011	2013-07-19	Special (immediate Track)
S010
S009	2012-11-30	30-day Notice
S008	2012-08-31	Normal 180 Day Track
S007
S006	2012-02-29	30-day Notice
S005	2012-02-02	30-day Notice
S004	2012-02-02	30-day Notice
S003	2012-02-02	30-day Notice
S002	2012-01-31	135 Review Track For 30-day Notice
S001	2012-01-31	Normal 180 Day Track No User Fee

NIH GUDID Devices

Device ID	PMA	Supp
07613336153932	P110022	022