P080003S002

None

FDA Premarket Approval P080003 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: P080003S002
• Classification Name: None
• PMA: P080003
• Supplement: S002

Supplemental Filings

Supplement Number	Date	Supplement Type
P080003		Original Filing
S008	2019-04-04	Normal 180 Day Track
S007	2018-05-02	Real-time Process
S006	2017-09-15	Normal 180 Day Track
S005	2017-05-02	Special (immediate Track)
S004	2017-03-30	Special (immediate Track)
S003	2016-03-30	Normal 180 Day Track
S002
S001	2012-10-09	Panel Track

NIH GUDID Devices

Device ID	PMA	Supp
15420045508033	P080003	000
15420045512696	P080003	000
15420045512474	P080003	000
15420045510388	P080003	000
15420045511897	P080003	000
15420045512313	P080003	000
15420045510395	P080003	000
15420045500013	P080003	000
15420045507272	P080003	000
15420045507289	P080003	000
15420045507296	P080003	000
15420045508019	P080003	000
15420045508026	P080003	000
15420045512689	P080003	000
15420045500020	P080003	001