P040025S002

None

FDA Premarket Approval P040025 S002

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: P040025S002
• Classification Name: None
• PMA: P040025
• Supplement: S002

Supplemental Filings

Supplement Number	Date	Supplement Type
P040025		Original Filing
S014	2013-06-26	Normal 180 Day Track No User Fee
S013	2013-05-28	Normal 180 Day Track
S012	2012-01-26	Real-time Process
S011	2010-09-29	Real-time Process
S010	2010-05-03	Real-time Process
S009	2009-07-21	Real-time Process
S008	2008-10-27	Real-time Process
S007	2008-07-16	Normal 180 Day Track
S006	2007-10-24	Real-time Process
S005	2007-08-24	30-day Notice
S004
S003
S002
S001

NIH GUDID Devices

Device ID	PMA	Supp
00382830016308	P040025	000
00382830009584	P040025	000
00382830009577	P040025	000
00382830009560	P040025	000
00382830004169	P040025	000