P140013S008

None

FDA Premarket Approval P140013 S008

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: P140013S008
• Classification Name: None
• PMA: P140013
• Supplement: S008

Supplemental Filings

Supplement Number	Date	Supplement Type
P140013		Original Filing
S013	2021-12-23	30-day Notice
S012	2020-11-25	Real-time Process
S011	2020-01-13	Normal 180 Day Track No User Fee
S010	2018-04-09	Real-time Process
S009	2018-01-31	Real-time Process
S008
S007	2017-04-03	Real-time Process
S006	2017-02-07	Normal 180 Day Track No User Fee
S005	2016-10-04	Normal 180 Day Track
S004	2016-09-20	Normal 180 Day Track No User Fee
S003	2016-07-05	Real-time Process
S002	2016-04-08	Normal 180 Day Track No User Fee
S001	2015-12-28	Real-time Process

NIH GUDID Devices

Device ID	PMA	Supp
00862393000162	P140013	000
00862393000155	P140013	000
00862393000131	P140013	000
00862393000117	P140013	000
00862393000148	P140013	000
00862393000148	P140013	012
00862393000117	P140013	012
00862393000162	P140013	012
00862393000100	P140013	012
00862393000131	P140013	012