P060023S007

None

FDA Premarket Approval P060023 S007

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

DeviceP060023S007
Classification NameNone
Applicant
PMAP060023
SupplementS007

Supplemental Filings

Supplement NumberDateSupplement Type
P060023Original Filing
S008 2019-10-18 Normal 180 Day Track No User Fee
S007
S006 2017-07-13 Normal 180 Day Track No User Fee
S005 2016-07-11 30-day Notice
S004 2012-12-13 30-day Notice
S003 2012-05-04 135 Review Track For 30-day Notice
S002 2011-04-15 135 Review Track For 30-day Notice
S001 2010-05-18 Normal 180 Day Track

NIH GUDID Devices

Device IDPMASupp
00613994365354 P060023 000
00613994181213 P060023 000
00613994181220 P060023 000
00613994181237 P060023 000
00613994181244 P060023 000
00613994181206 P060023 000
00613994365347 P060023 000
00613994365330 P060023 000
00613994365323 P060023 000
00613994365316 P060023 000
00613994363817 P060023 001
00613994360717 P060023 001
00613994363602 P060023 001
00613994363619 P060023 001
00613994363626 P060023 001
00613994363633 P060023 001
00613994363824 P060023 001
00613994363787 P060023 001
00613994363794 P060023 001
00613994363800 P060023 001
00613994363640 P060023 001

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