P050033S010

None

FDA Premarket Approval P050033 S010

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: P050033S010
• Classification Name: None
• PMA: P050033
• Supplement: S010

Supplemental Filings

Supplement Number	Date	Supplement Type
P050033		Original Filing
S020	2015-09-29	Special (immediate Track)
S019	2015-03-12	30-day Notice
S018	2015-01-29	135 Review Track For 30-day Notice
S017	2014-05-01	30-day Notice
S016	2014-05-01	Real-time Process
S015	2012-05-04	135 Review Track For 30-day Notice
S014	2011-12-23	Special (immediate Track)
S013	2011-06-20	Normal 180 Day Track No User Fee
S012	2011-04-12	135 Review Track For 30-day Notice
S011	2010-11-03	30-day Notice
S010
S009	2010-08-04	Special (immediate Track)
S008	2009-09-08	Special (immediate Track)
S007	2009-05-15	Normal 180 Day Track No User Fee
S006	2009-02-18	Normal 180 Day Track No User Fee
S005	2007-09-19	Normal 180 Day Track No User Fee
S004	2007-09-17	Real-time Process
S003	2007-09-06	135 Review Track For 30-day Notice
S002	2007-05-31	Normal 180 Day Track No User Fee
S001	2007-01-03	Normal 180 Day Track

NIH GUDID Devices

Device ID	PMA	Supp
00866142000014	P050033	000
00866142000007	P050033	000