P030029S002

None

FDA Premarket Approval P030029 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: P030029S002
• Classification Name: None
• PMA: P030029
• Supplement: S002

Supplemental Filings

Supplement Number	Date	Supplement Type
P030029		Original Filing
S013	2012-03-26	Normal 180 Day Track No User Fee
S012	2011-02-16	30-day Notice
S011	2010-09-29	30-day Notice
S010
S009	2009-09-28	Normal 180 Day Track
S008	2009-08-21	30-day Notice
S007	2009-05-18	Normal 180 Day Track
S006	2009-03-31	Normal 180 Day Track
S005	2009-03-03	Normal 180 Day Track No User Fee
S004	2008-09-18	Normal 180 Day Track
S003	2008-08-11	Normal 180 Day Track
S002
S001	2007-03-14	135 Review Track For 30-day Notice

NIH GUDID Devices

Device ID	PMA	Supp
00630414471860	P030029	000
00630414471914	P030029	003