P170018S005

None

FDA Premarket Approval P170018 S005

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

DeviceP170018S005
Classification NameNone
Applicant
PMAP170018
SupplementS005

Supplemental Filings

Supplement NumberDateSupplement Type
P170018Original Filing
S006 2020-04-23 30-day Notice
S005
S004 2019-09-11 Real-time Process
S003 2019-01-15 Real-time Process
S002 2019-01-11 Real-time Process
S001 2018-12-31 30-day Notice

NIH GUDID Devices

Device IDPMASupp
00883873790687 P170018 000
00883873790687 P170018 000
00883873790687 P170018 000
00883873824078 P170018 002
00883873824061 P170018 002
00883873824139 P170018 002
00883873824122 P170018 002
00883873824115 P170018 002
00883873824108 P170018 002
00883873824092 P170018 002
00883873824085 P170018 002
00883873824078 P170018 002
00883873824061 P170018 002
00883873824085 P170018 002
00883873824092 P170018 002
00883873824122 P170018 002
00883873824115 P170018 002
00883873824108 P170018 002
00883873824092 P170018 002
00883873824085 P170018 002
00883873824078 P170018 002
00883873824061 P170018 002
00883873824139 P170018 002
00883873824122 P170018 002
00883873824115 P170018 002
00883873824108 P170018 002
00883873824139 P170018 002

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