P130001S006

None

FDA Premarket Approval P130001 S006

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: P130001S006
• Classification Name: None
• PMA: P130001
• Supplement: S006

Supplemental Filings

Supplement Number	Date	Supplement Type
P130001		Original Filing
S007	2021-06-21	Real-time Process
S006
S005	2019-08-06	30-day Notice
S004	2018-02-20	30-day Notice
S003
S002	2016-05-10	Normal 180 Day Track No User Fee
S001	2016-04-29	Normal 180 Day Track No User Fee

NIH GUDID Devices

Device ID	PMA	Supp
04260400670036	P130001	000
04260400670029	P130001	000
04260400670012	P130001	000