P060025S002

None

FDA Premarket Approval P060025 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

DeviceP060025S002
Classification NameNone
Applicant
PMAP060025
SupplementS002

Supplemental Filings

Supplement NumberDateSupplement Type
P060025Original Filing
S014 2015-02-09 Normal 180 Day Track No User Fee
S013 2013-10-31 Normal 180 Day Track No User Fee
S012 2013-07-09 Real-time Process
S011 2013-03-05 Special (immediate Track)
S010 2013-02-22 Real-time Process
S009 2012-04-30 Normal 180 Day Track No User Fee
S008 2011-11-23 30-day Notice
S007 2010-09-17 30-day Notice
S006 2010-05-21 Special (immediate Track)
S005 2010-05-14 Normal 180 Day Track No User Fee
S004 2009-02-09 30-day Notice
S003 2009-01-05 Real-time Process
S002
S001 2008-10-31 30-day Notice

NIH GUDID Devices

Device IDPMASupp
00613994868268 P060025 000
00613994961587 P060025 000
00613994961594 P060025 000
00613994961600 P060025 000
00613994961617 P060025 000
00613994961624 P060025 000
00643169072503 P060025 000
00643169072510 P060025 000
00643169072527 P060025 000
00643169072534 P060025 000
00643169072541 P060025 000
00643169072558 P060025 000
00613994868213 P060025 000
00613994868220 P060025 000
00613994868237 P060025 000
00613994868244 P060025 000
00613994868251 P060025 000
00613994959720 P060025 000

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