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

DeviceP050033S010
Classification NameNone
Applicant
PMAP050033
SupplementS010

Supplemental Filings

Supplement NumberDateSupplement Type
P050033Original 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 IDPMASupp
00866142000014 P050033 000
00866142000007 P050033 000

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