P060023S007

None

FDA Premarket Approval P060023 S007

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: P060023S007
• Classification Name: None
• PMA: P060023
• Supplement: S007

Supplemental Filings

Supplement Number	Date	Supplement Type
P060023		Original Filing
S008	2019-10-18	Normal 180 Day Track No User Fee
S007
S006	2017-07-13	Normal 180 Day Track No User Fee
S005	2016-07-11	30-day Notice
S004	2012-12-13	30-day Notice
S003	2012-05-04	135 Review Track For 30-day Notice
S002	2011-04-15	135 Review Track For 30-day Notice
S001	2010-05-18	Normal 180 Day Track

NIH GUDID Devices

Device ID	PMA	Supp
00613994365354	P060023	000
00613994181213	P060023	000
00613994181220	P060023	000
00613994181237	P060023	000
00613994181244	P060023	000
00613994181206	P060023	000
00613994365347	P060023	000
00613994365330	P060023	000
00613994365323	P060023	000
00613994365316	P060023	000
00613994363817	P060023	001
00613994360717	P060023	001
00613994363602	P060023	001
00613994363619	P060023	001
00613994363626	P060023	001
00613994363633	P060023	001
00613994363824	P060023	001
00613994363787	P060023	001
00613994363794	P060023	001
00613994363800	P060023	001
00613994363640	P060023	001