P160032S005

None

FDA Premarket Approval P160032 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

• Device: P160032S005
• Classification Name: None
• PMA: P160032
• Supplement: S005

Supplemental Filings

Supplement Number	Date	Supplement Type
P160032		Original Filing
S010	2021-06-14	Real-time Process
S009	2020-07-27	Real-time Process
S008	2020-07-21	Real-time Process
S007	2020-05-26	30-day Notice
S006	2020-05-08	30-day Notice
S005
S004	2020-01-27	Real-time Process
S003
S002
S001	2018-11-09	30-day Notice

NIH GUDID Devices

Device ID	PMA	Supp
00815098020195	P160032	000