P010059S005

None

FDA Premarket Approval P010059 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: P010059S005
• Classification Name: None
• PMA: P010059
• Supplement: S005

Supplemental Filings

Supplement Number	Date	Supplement Type
P010059		Original Filing
S006	2016-08-02	Normal 180 Day Track No User Fee
S005
S004	2011-11-08	Normal 180 Day Track
S003	2007-03-19	Real-time Process
S002	2004-08-03	Normal 180 Day Track
S001	2004-01-20	Normal 180 Day Track No User Fee

NIH GUDID Devices

Device ID	PMA	Supp
04048509620004	P010059	007