P050031S008

None

FDA Premarket Approval P050031 S008

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

• Device: P050031S008
• Classification Name: None
• PMA: P050031
• Supplement: S008

Supplemental Filings

Supplement Number	Date	Supplement Type
P050031		Original Filing
S009	2022-04-15	30-day Notice
S008
S007	2020-08-05	30-day Notice
S006	2020-08-04	30-day Notice
S005	2019-03-13	Normal 180 Day Track No User Fee
S004
S003	2019-02-04	Real-time Process
S002
S001	2010-10-25	Normal 180 Day Track No User Fee

NIH GUDID Devices

Device ID	PMA	Supp
B22222	P050031	000
B22221	P050031	000