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Concentric Medical, Inc.

FDA 510(k) & PMA Approved Devices — 39 products

Total Devices39
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K173352 Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)POL2018-02-15 View
510(k) K131437 MODIFIED CONCENTRIC MICROCATHETERDQO2013-10-11 View
510(k) K131492 MODIFIED FLOWGATE BALLOON GUIDE CATHETERDQY2013-10-03 View
510(k) K122581 MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254DQY2012-11-21 View
510(k) K122478 MODIFIED TREVO RETRIEVERNRY2012-10-31 View
510(k) K120961 TREVO RETRIEVERNRY2012-08-03 View
510(k) K112404 CONCENTRIC BALLOON GUIDE CATHETERDQY2012-03-15 View
510(k) K113260 MODIFIED CONCENTIRC MICROCATHETERDQO2012-03-09 View
510(k) K111619 MODIFIED CONCENTRIC MICROCATHETERDQO2011-07-06 View
510(k) K110483 MODIFIED HD GUIDE CATHETERDQY2011-04-04 View
510(k) K093610 MODIFIED RETRIEVER (MODIFIED, LINE EXTENSION), MODELS 90152, 90153NRY2011-02-17 View
510(k) K102657 CONCENTRIC BALLOON GUIDE CATHETERDQY2010-11-17 View
510(k) K092298 MODIFICATION TO MODIFIED HD GUIDE CATHETERDQY2009-11-05 View
510(k) K091703 HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131QEZ2009-10-14 View
510(k) K091961 MODIFIED CONCENTRIC MICROCATHETER, MODEL 90047DQO2009-07-30 View
510(k) K090335 HD GUIDE CATHETERDQY2009-05-06 View
510(k) K090085 MERCI RETRIEVER, MODELS 90050, 90060, 90066, 90070, 90110, 90111, 90112, 90113NRY2009-02-12 View
510(k) K082034 MODIFICATION TO MERCI RETRIEVERNRY2008-08-15 View
510(k) K080583 MODIFIED HD GUIDE CATHETERDQY2008-07-18 View
510(k) K081305 MERCI RETRIEVERNRY2008-06-05 View
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