P030049S009

None

FDA Premarket Approval P030049 S009

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: P030049S009
• Classification Name: None
• PMA: P030049
• Supplement: S009

Supplemental Filings

Supplement Number	Date	Supplement Type
P030049		Original Filing
S016	2020-12-22	Real-time Process
S015	2020-07-31	30-day Notice
S014	2020-02-21	30-day Notice
S013	2019-09-27	30-day Notice
S012	2015-06-11	30-day Notice
S011	2014-07-10	Real-time Process
S010	2012-03-26	Normal 180 Day Track No User Fee
S009
S008	2010-04-06	30-day Notice
S007	2009-05-18	Normal 180 Day Track
S006	2009-05-12	30-day Notice
S005	2009-03-31	Normal 180 Day Track
S004	2009-03-09	Normal 180 Day Track No User Fee
S003	2009-02-04	30-day Notice
S002	2008-07-30	Normal 180 Day Track
S001

NIH GUDID Devices

Device ID	PMA	Supp
00630414472881	P030049	000
00630414472874	P030049	002
00630414472867	P030049	002