Medical Device Manufacturer · US , Moutian View , CA

Concentric Medical, Inc. - FDA 510(k) Cleared Devices

45 submissions · 44 cleared · Since 2001

Recent clearances: Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)

45

Total

44

Cleared

1

Denied

FDA 510(k) Regulatory Record - Concentric Medical, Inc. Cardiovascular ✕

27 devices

1-12 of 27

Cleared Feb 25, 2014

MODIFIED HD GUIDE CATHETER

Cardiovascular · 131d

Cleared Oct 11, 2013

MODIFIED CONCENTRIC MICROCATHETER

Cardiovascular · 144d

Cleared Oct 03, 2013

MODIFIED FLOWGATE BALLOON GUIDE CATHETER

Cardiovascular · 133d

Cleared Nov 21, 2012

MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254

Cardiovascular · 90d

Cleared Mar 15, 2012

CONCENTRIC BALLOON GUIDE CATHETER

Cardiovascular · 206d

Cleared Mar 09, 2012

MODIFIED CONCENTIRC MICROCATHETER

Cardiovascular · 126d

Cleared Jul 06, 2011

MODIFIED CONCENTRIC MICROCATHETER

Cardiovascular · 26d

Cleared Apr 04, 2011

MODIFIED HD GUIDE CATHETER

Cardiovascular · 45d

Cleared Nov 17, 2010

CONCENTRIC BALLOON GUIDE CATHETER

Cardiovascular · 63d

Cleared Nov 05, 2009

MODIFICATION TO MODIFIED HD GUIDE CATHETER

Cardiovascular · 99d

Cleared Oct 14, 2009

HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131

Cardiovascular · 126d

Cleared Jul 30, 2009

MODIFIED CONCENTRIC MICROCATHETER, MODEL 90047

Cardiovascular · 29d