P110011S011

None

FDA Premarket Approval P110011 S011

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

DeviceP110011S011
Classification NameNone
Applicant
PMAP110011
SupplementS011

Supplemental Filings

Supplement NumberDateSupplement Type
P110011Original Filing
S013 2016-08-17 135 Review Track For 30-day Notice
S012 2016-07-13 30-day Notice
S011
S010 2015-03-20 135 Review Track For 30-day Notice
S009 2015-02-12 135 Review Track For 30-day Notice
S008 2014-12-12 30-day Notice
S007 2014-03-18 30-day Notice
S006 2013-12-16 30-day Notice
S005 2013-11-15 30-day Notice
S004 2013-08-19 30-day Notice
S003 2013-07-01 30-day Notice
S002 2012-03-22 135 Review Track For 30-day Notice
S001 2011-11-14 30-day Notice

NIH GUDID Devices

Device IDPMASupp
00613994931283 P110011 000
00613994931146 P110011 000
00613994931139 P110011 000
00613994931122 P110011 000
00613994931115 P110011 000
00613994931108 P110011 000
00613994931092 P110011 000
00613994931085 P110011 000
00613994931078 P110011 000
00613994931061 P110011 000
00613994931054 P110011 000
00613994931047 P110011 000
00613994931153 P110011 000
00613994931160 P110011 000
00613994931276 P110011 000
00613994931269 P110011 000
00613994931252 P110011 000
00613994931245 P110011 000
00613994931238 P110011 000
00613994931221 P110011 000
00613994931214 P110011 000
00613994931207 P110011 000
00613994931191 P110011 000
00613994931184 P110011 000
00613994931177 P110011 000
00613994931030 P110011 000

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