P170006S013

None

FDA Premarket Approval P170006 S013

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

DeviceP170006S013
Classification NameNone
Applicant
PMAP170006
SupplementS013

Supplemental Filings

Supplement NumberDateSupplement Type
P170006Original Filing
S021 2022-07-20 30-day Notice
S020 2022-02-28 30-day Notice
S019 2020-11-25 30-day Notice
S018 2020-10-02 Real-time Process
S017 2020-08-03 30-day Notice
S016 2019-09-26 Real-time Process
S015 2019-06-20 30-day Notice
S014 2019-05-31 30-day Notice
S013
S012 2019-05-03 30-day Notice
S011 2019-04-18 30-day Notice
S010 2019-01-29 30-day Notice
S009 2019-01-24 30-day Notice
S008 2018-11-21 30-day Notice
S007
S006 2018-07-27 30-day Notice
S005 2017-11-22 30-day Notice
S004 2017-10-23 30-day Notice
S003 2017-10-18 30-day Notice
S002
S001 2017-09-11 30-day Notice

NIH GUDID Devices

Device IDPMASupp
00643169983212 P170006 000
00643169983205 P170006 000
00643169983199 P170006 000
00643169983182 P170006 000
00643169983175 P170006 000
00643169983229 P170006 024

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