P110015S001

None

FDA Premarket Approval P110015 S001

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: P110015S001
• Classification Name: None
• PMA: P110015
• Supplement: S001

Supplemental Filings

Supplement Number	Date	Supplement Type
P110015		Original Filing
S010	2022-05-03	30-day Notice
S009
S008	2021-03-16	Real-time Process
S007	2021-02-23	30-day Notice
S006	2019-10-30	30-day Notice
S005	2019-03-05	135 Review Track For 30-day Notice
S004	2018-06-14	30-day Notice
S003
S002	2016-07-15	135 Review Track For 30-day Notice
S001

NIH GUDID Devices

Device ID	PMA	Supp
M763K0211	P110015	000