P180046S039

None

FDA Premarket Approval P180046 S039

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

DeviceP180046S039
Classification NameNone
Applicant
PMAP180046
SupplementS039

Supplemental Filings

Supplement NumberDateSupplement Type
P180046Original Filing
S064 2023-01-10 30-day Notice
S063
S062 2022-09-29 Normal 180 Day Track
S061 2022-09-19 Normal 180 Day Track
S060 2022-08-15 30-day Notice
S059 2022-08-11 30-day Notice
S058
S057 2022-06-30 30-day Notice
S056
S055 2022-04-15 30-day Notice
S054
S053
S052 2022-03-24 30-day Notice
S051 2022-02-07 30-day Notice
S050 2022-01-14 30-day Notice
S049 2022-01-05 30-day Notice
S048
S047 2021-12-15 30-day Notice
S046
S045 2021-12-07 30-day Notice
S044
S043 2021-10-27 30-day Notice
S042 2021-10-18 30-day Notice
S041
S040
S039
S038
S037 2021-04-26 30-day Notice
S036
S035
S034 2021-02-25 30-day Notice
S033 2021-02-16 30-day Notice
S032 2021-02-08 30-day Notice
S031 2021-02-01 30-day Notice
S030 2021-02-01 30-day Notice
S029 2021-01-25 30-day Notice
S028
S027
S026 2020-11-05 Real-time Process
S025
S024
S023 2020-10-06 30-day Notice
S022 2020-10-02 30-day Notice
S021 2020-08-24 30-day Notice
S020
S019 2020-07-02 30-day Notice
S018 2020-06-16 30-day Notice
S017 2020-06-12 30-day Notice
S016 2020-06-05 30-day Notice
S015
S014
S013
S012
S011 2020-04-02 Normal 180 Day Track
S010 2020-03-16 30-day Notice
S009 2020-03-11 30-day Notice
S008 2020-03-06 30-day Notice
S007 2020-03-06 30-day Notice
S006
S005 2020-01-31 30-day Notice
S004
S003 2020-01-17 30-day Notice
S002
S001

NIH GUDID Devices

Device IDPMASupp
10810005340486 P180046 000
10810005340431 P180046 015
10810005340424 P180046 015
10810005340455 P180046 038
10810005340479 P180046 056

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