P030022S007

None

FDA Premarket Approval P030022 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: P030022S007
• Classification Name: None
• PMA: P030022
• Supplement: S007

Supplemental Filings

Supplement Number	Date	Supplement Type
P030022		Original Filing
S049	2022-07-14	30-day Notice
S048	2022-06-06	30-day Notice
S047	2022-05-23	30-day Notice
S046
S045	2017-11-24	30-day Notice
S044	2017-07-19	30-day Notice
S043	2017-05-04	30-day Notice
S042	2016-12-19	Special (immediate Track)
S041	2016-11-23	Special (immediate Track)
S040	2016-10-17	Special (immediate Track)
S039	2016-09-19	Normal 180 Day Track No User Fee
S038	2016-07-15	Normal 180 Day Track No User Fee
S037	2016-07-07	Real-time Process
S036	2016-06-23	Special (immediate Track)
S035	2015-12-28	30-day Notice
S034	2015-11-24	30-day Notice
S033	2015-07-27	Normal 180 Day Track No User Fee
S032	2015-07-27	Real-time Process
S031	2014-09-12	30-day Notice
S030	2014-05-02	30-day Notice
S029	2013-12-20	30-day Notice
S028	2013-12-18	30-day Notice
S027	2013-11-12	135 Review Track For 30-day Notice
S026	2013-09-25	30-day Notice
S025	2013-06-06	Real-time Process
S024	2013-03-21	135 Review Track For 30-day Notice
S023	2013-02-19	135 Review Track For 30-day Notice
S022	2012-08-10	30-day Notice
S021	2012-02-01	135 Review Track For 30-day Notice
S020	2011-12-21	30-day Notice
S019	2011-07-14	30-day Notice
S018	2011-04-29	30-day Notice
S017	2010-10-18	135 Review Track For 30-day Notice
S016	2010-07-07	Real-time Process
S015	2010-07-02	135 Review Track For 30-day Notice
S014	2010-05-12	30-day Notice
S013	2009-08-12	30-day Notice
S012	2009-07-22	135 Review Track For 30-day Notice
S011	2008-11-28	30-day Notice
S010	2008-09-10	Normal 180 Day Track No User Fee
S009	2008-02-06	135 Review Track For 30-day Notice
S008	2007-10-02	Normal 180 Day Track
S007
S006	2007-05-31	135 Review Track For 30-day Notice
S005	2007-05-01	135 Review Track For 30-day Notice
S004	2006-04-20	135 Review Track For 30-day Notice
S003	2006-04-20	135 Review Track For 30-day Notice
S002	2006-02-14	135 Review Track For 30-day Notice
S001	2005-09-02	Real-time Process

NIH GUDID Devices

Device ID	PMA	Supp
03596010194435	P030022	000
00885556020258	P030022	000
00885556020432	P030022	000
00885556020494	P030022	000
00885556021644	P030022	000
00885556021064	P030022	000
00885556021453	P030022	000
00885556021415	P030022	000
00885556021316	P030022	000
00885556021248	P030022	000
00885556021071	P030022	000
00885556021002	P030022	000
00885556020975	P030022	000
00885556020869	P030022	000
00885556020838	P030022	000
00885556020678	P030022	000
00885556020074	P030022	000
00885556019993	P030022	000
03596010194480	P030022	000
03596010194497	P030022	000
03596010194466	P030022	000
03596010194503	P030022	000
03596010194459	P030022	000
03596010194510	P030022	000
03596010194527	P030022	000
00885556019726	P030022	000
00885556019801	P030022	000
00885556019818	P030022	000
03596010194442	P030022	000
03596010194473	P030022	000
00885556020661	P030022	008
00885556020531	P030022	008
20885556028500	P030022	008
00885556019849	P030022	008
00885556020241	P030022	008
00885556020685	P030022	008
20885556028692	P030022	008
20885556028296	P030022	008
20885556027879	P030022	008
20885556027732	P030022	008
00885556027646	P030022	008
20885556027381	P030022	008
20885556027251	P030022	008
00885556022894	P030022	008
20885556026988	P030022	008
00885556021552	P030022	008
00885556021309	P030022	008
00885556021750	P030022	008
00885556021927	P030022	008
00885556022047	P030022	008
00885556022115	P030022	008
00885556022313	P030022	008
00885556274415	P030022	025
00885556274866	P030022	025
00885556274910	P030022	025
00885556274965	P030022	025
00885556281390	P030022	025
00885556281444	P030022	025