P130025S001

None

FDA Premarket Approval P130025 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: P130025S001
• Classification Name: None
• PMA: P130025
• Supplement: S001

Supplemental Filings

Supplement Number	Date	Supplement Type
P130025		Original Filing
S003	2017-09-05	Real-time Process
S002	2015-12-28	Normal 180 Day Track
S001

NIH GUDID Devices

Device ID	PMA	Supp
19764496368300	P130025	004